Primary Device ID | 10840277406511 |
NIH Device Record Key | d95f521f-49a2-45ee-93f0-f5a26451f1cc |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Chromic Gut |
Version Model Number | 1242CG |
Company DUNS | 964053560 |
Company Name | RIVERPOINT MEDICAL, LLC |
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 | true |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00840277406514 [Primary] |
GS1 | 10840277406511 [Package] Contains: 00840277406514 Package: [12 Units] In Commercial Distribution |
GAL | Suture, Absorbable, Natural |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2025-02-05 |
Device Publish Date | 2025-01-28 |
10840277406801 | Suture |
10840277406795 | Suture |
10840277406788 | Suture |
10840277406771 | Suture |
10840277406764 | Suture |
10840277406757 | Suture |
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10840277406733 | Suture |
00840277406729 | Suture |
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10840277406665 | Suture |
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10840277406634 | Suture |
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10840277406610 | Suture |
10840277406603 | Suture |
10840277406597 | Suture |
10840277406580 | Suture |
10840277406573 | Suture |
10840277406566 | Suture |
10840277406559 | Suture |
10840277406542 | Suture |
10840277406535 | Suture |
10840277406528 | Suture |
10840277406511 | Suture |
10840277406504 | Suture |
10840277406498 | Suture |
10840277406481 | Suture |