
Text extracted from the exhibit documents filed with the FCC. Open a document above to read the original.
Operator’s Manual © 2011 BUFFALO FILTER® 595 Commerce Drive Buffalo, New York USA 14228 (716) 835-7000 or (716) 835-3414 fax Division of Medtek Devices, Inc. Customer Service: 800-343-2324 (U.S. Only) – www.buffalofilter.com 1-716-835-7000 (International) Buffalo Filter ViroVac™ Operator’s Manual: Page 1 For a period of one (1) year following the date of delivery, BUFFALO FILTER warrants the Viro- Vac™ against any defects in material or workmanship. BUFFALO FILTER will repair or replace (at BUFFALO FILTER’S option) the same without charge, provided that routine maintenance as specified in this manual has been performed using replacement parts approved by BUFFALO FILTER. This warranty is void if the product is used in a manner or for purposes other than intended. © 2011 BUFFALO FILTER® Buffalo, New York USA 14228 (716) 835-7000 www.buffalofilter.com Division of Medtek Devices, Inc. Customer Service: 800-343-2324 (U.S. Only) 1-716-835-7000 (International) The revision level of this manual is specified by the highest revision letter found on either the inside front cover or enclosed errata pages (if any). Manual Number 901837 Unit Serial Number ______________________ 9D93 MEDICAL EQUIPMENT WITH RESPECT TO ELECTRICAL SHOCK, FIRE AND MECHANICAL HAZARDS ONLY IN ACCORDANCE WITH UL 60601-1 AND CAN/CSA C22.2 NO. 601.1 This device complies with Part 15 of the FCC Rules. Operation is subject to the following two conditions: (1) this device may not cause harmful interference and (2) this device must accept any interference received, including interference that may cause undesired operation. Buffalo Filter ViroVac™ Operator’s Manual: Page 2 Section Title Page 1.0 SYSTEM DESCRIPTION 3 1.1 Introduction 1.2 Inspection 1.3 Operational Information 1.4 Cautions and Warnings 2.0 OPERATING INSTRUCTIONS 10 2.1 System Controls 2.2 ViroSafe® Filter Instructions 2.3 Set-up and Operation 2.4 Specifications 3.0 MAINTENANCE 21 3.1 General Maintenance Information 3.2 Cleaning 3.3 Periodic Inspection 3.4 Troubleshooting 4.0 CUSTOMER SERVICE 22 4.1 Equipment Return 4.2 Ordering Information 5.0 TERMS & WARRANTY 23 Figure Title Page 1 Control Panel 14 Table of Contents & List of Illustrations Buffalo Filter ViroVac™ Operator’s Manual: Page 3 1.1 Introduction BUFFALO FILTER® ViroVac™ Smoke Evacuation Systems are designed to remove smoke and noxious odors produced by surgical smoke during laser, electrosurgical, ultrasonic, argon, plasma and mechanical instrument procedures. The ViroVac™ Smoke Evacuation Systems have been designed with a high suction, high flow rate centrifugal action pump. The ultra-quiet motor is used to draw the surgical smoke from the surgical site through the vacuum tubing and into the ViroSafe filter where the surgical smoke is processed by a series of filters. A single disposable filter is used to simplify the installation and removal during filter changes. The filter is completely enclosed to protect the healthcare person- nel from potential contamination during filter changes. One Buffalo Filter ViroSafe filter contains four different stages within to capture the smoke plume. The first stage filtration is a prefilter whose function is to trap and remove gross particulate and casual fluid. The second stage filtration is ULPA grade (Ultra Low Penetration Air) filter whose high-tech patented (U.S. Patent #5874052) design captures particulates and micro-organisms from .1 to .2 microns at an efficiency of 99.999%. The third stage filtration uses the highest grade virgin activated carbon, especially designed for Buffalo Filter for the removal and adsorption of odors and toxic gases produced by burning tis- sues. These harmful gases may constitute a health hazard to healthcare professionals who are subjected to prolonged exposure. The activated carbon used in the ViroVac™ Smoke Evacuation Systems preferentially removes toxic organic gases rather than water vapor and provides optimal odor removal. The fourth stage filtration is an expanded foam used to trap activated carbon fines from migrating out of the filter. The electronic controls on the face panel of the ViroVac™ Smoke Evacuation System has been designed “user friendly” and facilitate unit set up and operation. Please refer to Section 2.0 for Operating Instructions. 1.2 Inspection The ViroVac™ Smoke Evacuator has been thoroughly tested and inspected before shipment from the factory. Please check the unit before using it to insure that no damage has occurred in transit. If damage is evident, please contact BUFFALO FILTER Customer Service at 1-800-343-2324 (US Only) or (716) 835-7000 (International) System Description Section 1.0 Buffalo Filter ViroVac™ Operator’s Manual: Page 4 In addition, please compare the accessories you receive with the standard accessories list below. If an item is missing, please notify BUFFALO FILTER Customer Service. Standard Accessories: • Operator’s Manual • Power Cord • Pneumatic Footswitch Please contact BUFFALO FILTER Customer Service to purchase the following accessories: • Replacement Filters • Remote Switch Activator • Hoses, Tubing, Laparoscopic Kits, Adapters, Wands & Other Accessories 1.3 Operational Information The operational information contained in this section is intended for the customer review of regulatory issues. The information pertains to the use of the products both domestically and internationally: 1. The BUFFALO FILTER ViroVac™ Smoke Evacuation System(s) complies with IEC60601.1 electrical specifications in the following systems: 100/120 VAC 50/60 Hz, 220/240 VAC 50/60 Hz 2. Type of protection against electrical shock (UL 60601-1, Clause 5.1): Class I 3. Degree of protection against electric shock (UL 60601-1, Clause 5.2); Type CF Applied Part 4. Degree of protection against ingress of water (UL 60601-1, Clause 5.3): IPX1 5. Method of sterilization or disinfection recommended by BUFFALO FILTER (UL 60601-1, Clause 5.4): Unplug Unit. Wipe unit with a damp cloth containing mild disinfectant solution o…
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Side view Front view Side view Rear view
Part: VV120 Serial: Remote Activator CLEANING INSTRUCTIONS: UNPLUG UNIT - Wipe with damp cloth containing mild disinfectant solution, or soapy water. Wipe dry with a clean cloth. DO NOT STEAM STERILIZE. This device complies with Part 15 of the FCC Rules. Operation is subject to the following two conditions: (1) this device may not cause harmful interference, and (2) this device must accept any interfer- ence received, including interference that may cause undesired operation. Medical Equipment with respect to electrical shock, re and mechanical hazards only. In accordance with UL 60601-1 and CAN/CSA C22.2 NO. 601.1. 100/120V~ 10 Amps 50/60 Hz CAUTION Grounding reliability can only be achieved when the equipment is connected to a receptacle marked “Hospital Grade” or “Hospital Only”. CAUTION This contains a RFID wireless tag FCC ID: Y92-BF0002 and IC 9532A-BF0002.
24 33 1 16 16 9 25 17 9 26 7 11 11 11 11 6 15 15 6 6 15 15 6 34902076MOTOR BOOT ASY BACK VV 1 33902135LBL SN/MFG VIROVAC 1 32900190CABLE TIE 3 31901291RFID TAPE 1 30901286RFID ANTENNA 24" 1 29902131WIRE KIT VIROVAC 1 28902117LBL GROUND STUD 1 27901175PCB HARNESS 35 1 26901174PCB HARNESS 33 1 25901254GROUND LUG POAG S5/25 1 24901880LBL SERIAL LABEL VV 120 1 23901468WIRE MANAGE CLIP 1 22902120FERRITE 25-300MHZ 1 21901793MOTOR 120V PAN SMALL 1 20902092INSUL 3 VV 5 19901939INSUL 2 VV 1 18901938INSUL 1 VV 1 17901792POWER ENTRY MOD VV 1 16902099SCREW 6-32 5/16 PH FH SS 16 15901315BOLT 10-32 1/2 PPSS 4 14902097S 6-32 .25IN PH PN STF SS 1 13902098SCREW 3-24 5/8 PH PN PL SS 2 12901140NUT 6-32 W/WASHER SS 4 11901323B 6-32 .25 PH PN S ZP 4 10901132NUT .25-20 W/WASHER SS 2 9901146M6 NUT WITH TOOTH WASHER 2 8901791KEYPAD VV 1 7901800PCB RFID VIROVAC 120 1 6901300RUBBER FEET RV 4 5901795FILTER BASKET VV 1 4901789Motor Boot Front VV 1 3901796FASCIA VV 1 2901787HOUSING TOP VV 1 1901788HOUSING BOTTOM VV 1 ITEM NO. PART NO.DESCRIPTION base assembly/QTY. BILL OF MATERIALS REVISIONS REV.DESCRIPTIONDATECHGD BYEC# -See Sheet1--- D C B A A B C D 1 2 3 4 5 6 7 8 8 7 6 5 4 3 2 1 TOLERANCE UNLESS SPECIFIED: FRACTIONAL N/A ANGULAR 0.5 .XX 0.01 .XXX 0.005 DIMENSIONING IS PER ANSI Y14.5 ALL DIMENSIONS ARE IN INCHES UNLESS OTHERWISE SPECIFIED THIRD ANGLE PROJECTION THE INFORMATION CONTAINED IN THIS DRAWING IS THE SOLE PROPERTY OF BUFFALO FILTER - MEDTEK DEVICES. ANY REPRODUCTION IN PART OR AS A WHOLE WITHOUT THE WRITTEN PERMISSION OF BUFFALO FILTER - MEDTEK DEVICES IS PROHIBITED. PROPRIETARY AND CONFIDENTIAL FINISH: N/A MATERIAL: N/A DRAWN ENG APPR. DATE NAME TITLE: SIZE B DWG. NO.REV SCALE: 1:2 DEV1 3/11/2011 SHEET 4 OF 6 300235 DO NOT SCALE DRAWING DCO VIROVAC SUB ASSEMBLY
Complete internal appearance Top modular Bottom modular Zoom in on modular board Antenna and Location Motor filter cover Reader location Antenna location Motor View Motor view side Motor view top Motor view bottom
Underwriters Laboratories Inc. A not-for-profit organization dedicated 1285 Walt Whitman Rd. to public safety and committed to Melville, NY 11747 quality service for over 100 years Tel: (631) 271-6200 Fax: (631)439-6095 Underwriters Laboratories Inc. 1285 Walt Whitman Rd. Melville, NY 11747 www.ul.com/emc (631) 271-6200 Job Number: 1001291463 Project Number: 10ME09079 File Number: E174420 Revision Date: 2011- 05-03 Model: FCC ID: Industry Canada ID: 901879 Y92-BF0002 9532A-BF0002 Electromagnetic Compatibility Test Report For BUFFALO FILTER, DIV OF MEDTEK DEVICES INC Copyright    2010 Underwriters Laboratories Inc. Underwriters Laboratories Inc. authorizes the above-named company to reproduce this Report provided it is reproduced in its entirety. Job Number: 1001291463 File Number: E174420 Page 2 of 50 Model Number: 901879 Client Name: BUFFALO FILTER, DIV OF MEDTEK DEVICES INC FCC ID: Y92-BF0002 Industry Canada 9532A-BF002 Underwriters Laboratories Inc. 1285 Walt Whitman Rd. Melville, New York 11747 USA Tel.: 631 271-6200 Fax: 631 439-6095 Rev. No 1.0 EMC Report 2010-87-EM-F0042 Test Report Details Tests Performed By: Underwriters Laboratories Inc. 1285 Walt Whitman Rd. Melville, NY 11747 Tests Performed For: BUFFALO FILTER, DIV OF MEDTEK DEVICES INC 595 COMMERCE DRIVE BUFFALO , NY 14228 Applicant Contact: Tony Lizauckas Title: Program Manager - New Product Development Phone: 1-800-343-2324 ext 227 Fax: (716) 691-5056 E-mail: [email protected] Test Report Revision Date: 2011-05-03 Product Type: Limited Modular RFID Tag (installed in Smoke Evacuator Systems) Product standards FCC Part 15, Subpart C, 15.225, RSS-210, RSS-GEN Model Number: 901879 Sample Part Number: Not provided at time of test EUT Category: Low Power RFID 13.56MHz Testing Start Date: 2011-02-18 Date Testing Complete: 2011-03-04 Overall Results: Compliant Underwriters Laboratories Inc. reports apply only to the specific samples tested under stated test conditions. All samples tested were in good operating condition throughout the entire test program. It is the manufacturer's responsibility to assure that additional production units of this model are manufactured with identical electrical and mechanical components. Underwriters Laboratories Inc. shall have no liability for any deductions, inferences or generalizations drawn by the client or others from Underwriters Laboratories Inc. issued reports. This report shall not be used to claim, constitute or imply product certification, approval, or endorsement by NVLAP, NIST, A2LA, or any agency of the US government. This report may contain test results that are not covered by the NVLAP or A2LA accreditation. The scope of accreditation is limited to the specific tests that are listed on the NVLAP and/or A2LA websites referenced at the end of this report. Job Number: 1001291463 File Number: E174420 Page 3 of 50 Model Number: 901879 Client Name: BUFFALO FILTER, DIV OF MEDTEK DEVICES INC FCC ID: Y92-BF0002 Industry Canada 9532A-BF002 Underwriters Laboratories Inc. 1285 Walt Whitman Rd. Melville, New York 11747 USA Tel.: 631 271-6200 Fax: 631 439-6095 Rev. No 1.0 EMC Report 2010-87-EM-F0042 Report Directory 1.0 G E N E R A L - Product Description ..................................................................................................................4 1.1 Equipment Description ...................................................................................................................................4 1.2 Equipment Marking Plate ...............................................................................................................................4 1.3 Device Configuration During Test ..................................................................................................................5 1.3.1 Equipment Used During Test: ....................................................................................................................5 1.3.2 Input/Output Ports: .....................................................................................................................................5 1.3.3 EUT Internal Operating Frequencies: ........................................................................................................5 1.3.4 Power Interface: .........................................................................................................................................6 1.4 Block Diagram: ...............................................................................................................................................6 1.5 EUT Configurations ........................................................................................................................................7 1.6 EUT Operation Modes ....................................................................................................................................7 2.0 Summary ............................................................................................................................................................7 2.1 Deviations from standard test methods ..........................................................................................................7 2.2 Device Modifications Necessary for Compliance ...........................................................................................7 2.3 Reference Standards .....................................................................................................................................8 2.4 Results Summary ...........................................................................................................................................8 3.0 Calibration of Equipment Used for Measurement ..............................................................................................9 4.0 EMISSIONS TEST RESULTS ......................................................................................................................... 10 4.…
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Job Number: 1001291463 File Number: E174420 Page 12 of 50 Model Number: 901879 Client Name: BUFFALO FILTER, DIV OF MEDTEK DEVICES INC FCC ID: Y92-BF0002 Industry Canada 9532A-BF002 Underwriters Laboratories Inc. 1285 Walt Whitman Rd. Melville, New York 11747 USA Tel.: 631 271-6200 Fax: 631 439-6095 Rev. No 1.0 EMC Report 2010-87-EM-F0042 Figure 1 Test Setup for Conducted Emissions Model number depicted in the photo is the system model number the RFID modular internal model is 901879 Job Number: 1001291463 File Number: E174420 Page 19 of 50 Model Number: 901879 Client Name: BUFFALO FILTER, DIV OF MEDTEK DEVICES INC FCC ID: Y92-BF0002 Industry Canada 9532A-BF002 Underwriters Laboratories Inc. 1285 Walt Whitman Rd. Melville, New York 11747 USA Tel.: 631 271-6200 Fax: 631 439-6095 Rev. No 1.0 EMC Report 2010-87-EM-F0042 Figure 3 Test Setup for Occupied Bandwidth Model number depicted in the photo is the system model number the RFID modular internal model is 901879 Job Number: 1001291463 File Number: E174420 Page 23 of 50 Model Number: 901879 Client Name: BUFFALO FILTER, DIV OF MEDTEK DEVICES INC FCC ID: Y92-BF0002 Industry Canada 9532A-BF002 Underwriters Laboratories Inc. 1285 Walt Whitman Rd. Melville, New York 11747 USA Tel.: 631 271-6200 Fax: 631 439-6095 Rev. No 1.0 EMC Report 2010-87-EM-F0042 Figure 5 Test Setup for Frequency Stability Model number depicted in the photo is the system model number the RFID modular internal model is 901879 Job Number: 1001291463 File Number: E174420 Page 27 of 50 Model Number: 901879 Client Name: BUFFALO FILTER, DIV OF MEDTEK DEVICES INC FCC ID: Y92-BF0002 Industry Canada 9532A-BF002 Underwriters Laboratories Inc. 1285 Walt Whitman Rd. Melville, New York 11747 USA Tel.: 631 271-6200 Fax: 631 439-6095 Rev. No 1.0 EMC Report 2010-87-EM-F0042 Figure 6 Test setup for Radiated Emissions 9KHz to 30 MHz Vertical Polarity Front View 9KHz to 30 MHz Vertical Polarity Rear View Model number depicted in the photo is the system model number the RFID modular internal is 901879 Job Number: 1001291463 File Number: E174420 Page 28 of 50 Model Number: 901879 Client Name: BUFFALO FILTER, DIV OF MEDTEK DEVICES INC FCC ID: Y92-BF0002 Industry Canada 9532A-BF002 Underwriters Laboratories Inc. 1285 Walt Whitman Rd. Melville, New York 11747 USA Tel.: 631 271-6200 Fax: 631 439-6095 Rev. No 1.0 EMC Report 2010-87-EM-F0042 9KHz to 30 MHz Horizontal Polarity Front View 9KHz to 30 MHz Horizontal Polarity Rear View Model number depicted in the photo is the system model number the RFID modular internal is 901879 Job Number: 1001291463 File Number: E174420 Page 29 of 50 Model Number: 901879 Client Name: BUFFALO FILTER, DIV OF MEDTEK DEVICES INC FCC ID: Y92-BF0002 Industry Canada 9532A-BF002 Underwriters Laboratories Inc. 1285 Walt Whitman Rd. Melville, New York 11747 USA Tel.: 631 271-6200 Fax: 631 439-6095 Rev. No 1.0 EMC Report 2010-87-EM-F0042 Figure 7: Test Setup for Radiated Emissions Front View 30-1000MHz Rear View 30-1000MHz Model number depicted in the photo is the system model number the RFID modular internal is 901879
1285 Walt Whitman Road · Melville, New York · United States
| # | Rule Parts | Frequency Range | Power Output |
|---|---|---|---|
| 1 | 15C | 13.56 MHz - 13.56 MHz | - |

Buffalo Filter Limited Module RFID System
Equipment Class
DXX - Part 15 Low Power Communication Device Transmitter