| Primary Device ID | 20845854053062 |
| NIH Device Record Key | d31fdb61-6fe9-4cd5-8842-0fb2a6417702 |
| Commercial Distribution Status | In Commercial Distribution |
| Version Model Number | AV8570 |
| Catalog Number | AV8570 |
| Company DUNS | 071595540 |
| Company Name | Conmed Corporation |
| Device Count | 1 |
| DM Exempt | true |
| Pre-market Exempt | true |
| 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 |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 20845854053062 [Primary] |
| KQM | CAMERA, SURGICAL AND ACCESSORIES |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2020-07-31 |
| Device Publish Date | 2020-07-23 |
| 30653405033251 - ULTRACLEAN | 2026-03-25 ULTRACLEAN ACCESSORY ELECTRODE, 1 INCH COATED NEEDLE WITH EXTENDED INSULATION |
| 20845854035594 - CONCEPT | 2026-03-25 CONCEPT ABLATOR ELECTRODE, 90 DEGREE (ELECTRODE ONLY), QTY 5 |
| 30653405013925 - CONMED | 2026-03-24 ELECTROSURGICAL HANDPIECE SHEATH |
| 30653405014953 - POOLE | 2026-03-24 POOLE Suction Instrument with Removable Sheath and 10' (3.0 m) Clear Plastic Tubing |
| 30810175502367 - IBS-B | 2026-03-19 NON-BEVELED SCREWDRIVER T15- AO ATTACHMENT |
| 30653405546508 - Y-KnotlessTM Flex | 2026-02-16 Y-KnotlessTM Flex Anchor, Green/Black #2 Hi-Fi Suture, 1.8 mm |
| 30653405990721 - Y-KnotlessTM Flex | 2026-02-16 Y-KnotlessTM Flex Anchor, White/Black #2 Hi-Fi Suture, 1.8 mm |
| 10653405986362 - CONMED | 2026-01-26 Universal Modular Base Cart |