| Primary Device ID | 40653405081976 |
| NIH Device Record Key | e444663b-8284-450f-bb53-fadb398221de |
| Commercial Distribution Status | In Commercial Distribution |
| Version Model Number | AES-WFC |
| Catalog Number | AES-WFC |
| Company DUNS | 071595540 |
| Company Name | Conmed Corporation |
| Device Count | 1 |
| 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 | false |
| Serial Number | true |
| 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 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 20653405081972 [Primary] |
| GS1 | 30653405081979 [Primary] |
| GS1 | 40653405081976 [Direct Marking] |
| GEI | ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2018-03-29 |
| Device Publish Date | 2016-09-24 |
| 20653405000898 - CONMED | 2024-07-23 ADULT ECG BACKPAD |
| 20653405001123 - CONMED | 2024-07-23 INFANT ECG BACKPAD |
| 30653405050715 - CONMED | 2024-07-23 American Dilator, Reusable, 21F |
| 20653405051098 - Harrell | 2024-07-23 Harrell Bronchoscope Unsheathed Cytology Brush, No Handle, 7mm X 110cm |
| 20845854037147 - ULTRAFIX MICROMITE | 2024-07-23 ULTRAFIX MICROMITE DRILL, 1.8MM |
| 20845854037390 - CONMED | 2024-07-23 6MM SUTURE PUNCH, STRAIGHT, LOW PROFILE, NO. 2 MONOFILAMENT |
| 20845854037826 - OSTEOPREP | 2024-07-23 4MM CONVEX RASP, OSTEOPREP |
| 20845854650278 - Argo Knotless GENESYS | 2024-07-18 4.75mm Argo Knotless® GENESYSTM SP Anchor |