Primary Device ID | 20845854081287 |
NIH Device Record Key | 6a690ab3-92b2-4cef-ab10-cd45fdf89e95 |
Commercial Distribution Status | In Commercial Distribution |
Version Model Number | DCCOV01 |
Catalog Number | DCCOV01 |
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 | 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 | 00815198012502 [Previous] |
GS1 | 20845854081287 [Primary] |
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 | 2020-07-03 |
Device Publish Date | 2020-06-25 |
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10845854026809 - GENESYS CROSSFT | 2024-04-18 6.5MM CROSSFT-BC ANCHOR, W/DISP, DBL |
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