Primary Device ID | 00840277407313 |
NIH Device Record Key | e8b260b0-3d8b-4caa-8c9d-d4582f05fa01 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Mono-dox |
Version Model Number | M397 |
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 | 00840277407313 [Primary] |
GS1 | 10840277407310 [Package] Package: [12 Units] In Commercial Distribution |
NEW | Suture, Surgical, Absorbable, Polydioxanone |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2025-01-22 |
Device Publish Date | 2025-01-14 |
10840277407334 | Suture |
10840277407327 | Suture |
00840277407313 | Suture |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
MONO-DOX 76406679 2715469 Live/Registered |
CP MEDICAL 2002-05-10 |