CooperSurgical 395-703
GUDID 00845854081757
ULPA Charcoal Filter for MiniVac Smoke Evacuator
Conmed Corporation
Surgical plume evacuation system filter Surgical plume evacuation system filter Surgical plume evacuation system filter Surgical plume evacuation system filter Surgical plume evacuation system filter Surgical plume evacuation system filter Surgical plume evacuation system filter Surgical plume evacuation system filter Surgical plume evacuation system filter Surgical plume evacuation system filter Surgical plume evacuation system filter Surgical plume evacuation system filter Surgical plume evacuation system filter Surgical plume evacuation system filter Surgical plume evacuation system filter Surgical plume evacuation system filter Surgical plume evacuation system filter Surgical plume evacuation system filter Surgical plume evacuation system filter Surgical plume evacuation system filter Surgical plume evacuation system filter Surgical plume evacuation system filter Surgical plume evacuation system filter Surgical plume evacuation system filter Surgical plume evacuation system filter Surgical plume evacuation system filter Surgical plume evacuation system filter Surgical plume evacuation system filter Surgical plume evacuation system filter Surgical plume evacuation system filter Surgical plume evacuation system filter| Primary Device ID | 00845854081757 |
| NIH Device Record Key | b70e767a-ae07-4842-9c7e-99c537c3d8ee |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | CooperSurgical |
| Version Model Number | 395-703 |
| Catalog Number | 395-703 |
| Company DUNS | 071595540 |
| Company Name | Conmed Corporation |
| Device Count | 3 |
| 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 | true |
Customer Support Contacts
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00815198012649 [Previous] |
| GS1 | 00845854081757 [Unit of Use] |
| GS1 | 20845854081751 [Primary] |
FDA Product Code
| FYD | APPARATUS, EXHAUST, SURGICAL |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | false |
Device Entry Metadata
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2024-04-02 |
| Device Publish Date | 2024-03-25 |
Devices Manufactured by Conmed Corporation
| 30845854026797 - GENESYS CrossFT, Hi-Fi | 2024-04-25 5.5 mm GENESYS CrossFT Suture Anchor with Three #2 (5 metric) Hi-Fi Sutures |
| 30845854026803 - GENESYS CrossFT, Hi-Fi | 2024-04-25 6.5 mm GENESYS CrossFT Suture Anchor with Two #2 (5 metric) Hi-Fi Sutures |
| 30845854026810 - GENESYS CrossFT, Hi-Fi | 2024-04-25 6.5 mm GENESYS CrossFT Suture Anchor with Three #2 (5 metric) Hi-Fi Sutures |
| 30845854027862 - GENESYS PressFT, Hi-Fi | 2024-04-25 GENESYS PressFT 2.1 w/One #2 (5 metric) Hi-Fi Suture, HIP (1 White/Black) |
| 30845854027893 - GENESYS PressFT, Hi-Fi | 2024-04-25 GENESYS PressFT 2.6 w/One #2 (5 metric) Hi-Fi Suture, HIP (1 White/Black) |
| 30845854034600 - GENESYS CrossFT, Hi-Fi | 2024-04-25 GENESYS CrossFT 5.5 mm Suture Anchor, w/3 Hi-Fi #2 (5 metric) Sutures w/Needles |
| 30845854034617 - GENESYS CrossFT, Hi-Fi | 2024-04-25 GENESYS CrossFT 6.5 mm Suture Anchor, w/2 Hi-Fi #2 (5 metric) Sutures w/Needles |
| 30653405988643 - Argo Knotless GENESYS | 2024-04-22 5.5mm Argo Knotless® GENESYSTM Anchor |
Trademark Results [CooperSurgical]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 COOPERSURGICAL 85186600 4058824 Live/Registered |
CooperSurgical, Inc. 2010-11-29 |
 COOPERSURGICAL 74219286 1862209 Live/Registered |
COOPERSURGICAL, INC. 1991-11-06 |
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