| Primary Device ID | 00845854081795 |
| NIH Device Record Key | d51b0ea1-1c65-4d7f-828d-26534195db82 |
| Commercial Distribution Status | In Commercial Distribution |
| Version Model Number | VSSV50502 |
| Catalog Number | VSSV50502 |
| 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 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00845854081795 [Unit of Use] |
| GS1 | 20845854081799 [Primary] |
| GS1 | 30845854081796 [Package] Contains: 20845854081799 Package: Box [2 Units] In Commercial Distribution |
| FYD | APPARATUS, EXHAUST, SURGICAL |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2020-07-20 |
| Device Publish Date | 2020-07-12 |
| 20653405037573 - CONMED | 2026-04-01 PUNCTURE CLOSURE DEVICE |
| 10653405063797 - CONMED | 2026-04-01 CONMED ECG LEADWIRES, 5 LEADS, 28" |
| 00845854035590 - CONCEPT | 2026-04-01 CONCEPT ABLATOR ELECTRODE, 90 DEGREE (ELECTRODE ONLY), QTY 5 |
| 10845854041116 - POWERPRO | 2026-04-01 POWERPRO UNIVERSAL CONTROLLER 115V |
| 10845854041291 - CONMED | 2026-04-01 XENON REPLACEMENT BULB, 300 WATT |
| 00653405014952 - POOLE | 2026-04-01 POOLE Suction Instrument with Removable Sheath and 10' (3.0 m) Clear Plastic Tubing |
| 20653405017759 - CONMED | 2026-04-01 CABLE, SHIELD, 3 LEADS, CONN 3 |
| 20653405017766 - CONMED | 2026-04-01 ECG MONITOR CABLE |