| Primary Device ID | 30845854053120 |
| NIH Device Record Key | 8b448e89-703b-4944-b1df-61ec0326bad4 |
| Commercial Distribution Discontinuation | 2020-11-19 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Brand Name | MICROSAFE |
| Version Model Number | MGVS35302 |
| Catalog Number | MGVS35302 |
| Company DUNS | 071595540 |
| Company Name | Conmed Corporation |
| Device Count | 2 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | false |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | true |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Phone | +1(800)237-0169 |
| CUSTOMER_SERVICE@CONMED.COM | |
| Phone | +1(800)237-0169 |
| CUSTOMER_SERVICE@CONMED.COM | |
| Phone | +1(800)237-0169 |
| CUSTOMER_SERVICE@CONMED.COM | |
| Phone | +1(800)237-0169 |
| CUSTOMER_SERVICE@CONMED.COM | |
| Phone | +1(800)237-0169 |
| CUSTOMER_SERVICE@CONMED.COM | |
| Phone | +1(800)237-0169 |
| CUSTOMER_SERVICE@CONMED.COM | |
| Phone | +1(800)237-0169 |
| CUSTOMER_SERVICE@CONMED.COM | |
| Phone | +1(800)237-0169 |
| CUSTOMER_SERVICE@CONMED.COM | |
| Phone | +1(800)237-0169 |
| CUSTOMER_SERVICE@CONMED.COM | |
| Phone | +1(800)237-0169 |
| CUSTOMER_SERVICE@CONMED.COM | |
| Phone | +1(800)237-0169 |
| CUSTOMER_SERVICE@CONMED.COM | |
| Phone | +1(800)237-0169 |
| CUSTOMER_SERVICE@CONMED.COM | |
| Phone | +1(800)237-0169 |
| CUSTOMER_SERVICE@CONMED.COM | |
| Phone | +1(800)237-0169 |
| CUSTOMER_SERVICE@CONMED.COM | |
| Phone | +1(800)237-0169 |
| CUSTOMER_SERVICE@CONMED.COM | |
| Phone | +1(800)237-0169 |
| CUSTOMER_SERVICE@CONMED.COM | |
| Phone | +1(800)237-0169 |
| CUSTOMER_SERVICE@CONMED.COM | |
| Phone | +1(800)237-0169 |
| CUSTOMER_SERVICE@CONMED.COM |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00845854053129 [Unit of Use] |
| GS1 | 20845854053123 [Primary] |
| GS1 | 30845854053120 [Package] Contains: 20845854053123 Package: Box [2 Units] Discontinued: 2020-11-19 Not in Commercial Distribution |
| FYD | APPARATUS, EXHAUST, SURGICAL |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2022-11-07 |
| Device Publish Date | 2020-06-18 |
| 00845854053129 | MicroSafe Smoke Evacuation Filter with 1/4 Inch (6.4mm), 3/8 Inch (9.5mm), and 7/8 Inch (22mm) P |
| 10845854053119 | MicroSafe Smoke Evacuation Filter with 1/4 Inch (6.4mm), 3/8 Inch (9.5mm), and 7/8 Inch (22mm) P |
| 30845854053120 | MicroSafe Smoke Evacuation Filter with 1/4 Inch (6.4mm), 3/8 Inch (9.5mm), and 7/8 Inch (22mm) P |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() MICROSAFE 90458005 not registered Live/Pending |
MICROSAFE GROUP DMCC 2021-01-11 |
![]() MICROSAFE 87555727 not registered Dead/Abandoned |
Microsafe Group DMCC 2017-08-03 |
![]() MICROSAFE 87054911 not registered Dead/Abandoned |
Michael E. Reed 2016-05-31 |
![]() MICROSAFE 85518850 not registered Dead/Abandoned |
Michael Rothbard 2012-01-18 |
![]() MICROSAFE 85092897 4110867 Dead/Cancelled |
Koch Filter Corporation 2010-07-26 |
![]() MICROSAFE 78906106 3393343 Dead/Cancelled |
PROXY LABORATORIES B.V. 2006-06-12 |
![]() MICROSAFE 78597648 3356076 Live/Registered |
The Decor Corporation Pty Ltd 2005-03-29 |
![]() MICROSAFE 78235044 not registered Dead/Abandoned |
Vygon 2003-04-08 |
![]() MICROSAFE 78047531 2547437 Dead/Cancelled |
CNA Holdings, Inc. 2001-02-09 |
![]() MICROSAFE 77695695 not registered Dead/Abandoned |
Premier Foam, Inc. 2009-03-20 |
![]() MICROSAFE 76256827 not registered Dead/Abandoned |
DETCON Inc. 2001-05-14 |
![]() MICROSAFE 76243803 not registered Dead/Abandoned |
Anax Int'l Inc. 2001-04-23 |