Primary Device ID | 10840277406368 |
NIH Device Record Key | efbef12a-258d-4e99-af8d-a33494846eae |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Plain Gut |
Version Model Number | 820PG |
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 | 00840277406361 [Primary] |
GS1 | 10840277406368 [Package] Contains: 00840277406361 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 |
10840277406382 | Suture |
10840277406375 | Suture |
10840277406368 | Suture |
10840277406351 | Suture |
10840277406344 | Suture |
10840277406337 | Suture |
10840277406320 | Suture |
10840277406313 | Suture |
10840277406306 | Suture |
10840277406290 | Suture |
10840277406283 | Suture |
10840277406276 | Suture |
10840277406269 | Suture |
10840277406252 | Suture |
10840277406245 | Suture |
10840277406238 | Suture |
10840277406221 | Suture |