Primary Device ID | 20845854013578 |
NIH Device Record Key | 098873a3-4eaf-4686-9890-89a5d9e577f6 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ENDOPEARL |
Version Model Number | C8059 |
Catalog Number | C8059 |
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 | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | +1(800)237-0169 |
CUSTOMER_SERVICE@CONMED.COM | |
Phone | +1(800)237-0169 |
CUSTOMER_SERVICE@CONMED.COM |
Outer Diameter | 9 Millimeter |
Outer Diameter | 9 Millimeter |
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 | 20845854013578 [Primary] |
MAI | FASTENER, FIXATION, BIODEGRADABLE, SOFT TISSUE |
Steralize Prior To Use | true |
Device Is Sterile | true |
[20845854013578]
Ethylene Oxide
[20845854013578]
Ethylene Oxide
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 5 |
Public Version Date | 2019-03-21 |
Device Publish Date | 2016-09-24 |
20845854014292 | ENDOPEARL 7MM, SOFT TISSUE FIXATION DEVICE |
20845854013776 | ENDOPEARL 8MM, SOFT TISSUE FIXATION DEVICE |
20845854013578 | ENDOPEARL 9MM, SOFT TISSUE FIXATION DEVICE |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
ENDOPEARL 75585247 2400782 Live/Registered |
CONMED CORPORATION 1998-11-09 |