Primary Device ID | 10845854025536 |
NIH Device Record Key | c6df28a8-d695-4aaf-ad06-2c669be0ed0d |
Commercial Distribution Status | In Commercial Distribution |
Version Model Number | 8736 |
Catalog Number | 8736 |
Company DUNS | 071595540 |
Company Name | Conmed Corporation |
Device Count | 1 |
DM Exempt | false |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 10845854025536 [Primary] |
GS1 | 20845854025533 [Direct Marking] |
FZX | Guide, surgical, instrument |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-06-17 |
Device Publish Date | 2022-06-09 |
20653405003370 - CONMED | 2024-04-17 CONMED Accessory Electrode, 3/16 Inch (5 mm) Ball |
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20845854020590 - ULTRABLATOR | 2024-04-16 ULTRABLATOR 30 Degree, 60 mm length, 2.5 mm diameter |
20845854020613 - ULTRABLATOR | 2024-04-16 ULTRABLATOR 90 Degree, Three Rib, 130 mm length, 3.2 mm diameter |
20845854029548 - ULTRABLATOR | 2024-04-16 ULTRABLATOR 30 Degree, 110 mm length, 2.5 mm diameter |
20845854029555 - ULTRABLATOR | 2024-04-16 ULTRABLATOR 90 Degree, 110 mm length, 2.5 mm diameter |
20845854029562 - ULTRABLATOR | 2024-04-16 ULTRABLATOR 30 Degree, 110 mm length, 3.2 mm diameter |
10653405003854 - ABC | 2024-04-15 ABC PROBE 5 MM HANDSWITCHING PROBE, 36 CM |