Primary Device ID | 10810020084099 |
NIH Device Record Key | d96c38dd-db27-4d78-a1a1-0e9c2c7a0415 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | MICROSUTURE |
Version Model Number | GEM188BK |
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 | 00810020084092 [Primary] |
GS1 | 10810020084099 [Package] Contains: 00810020084092 Package: [12 Units] In Commercial Distribution |
GAR | Suture, Nonabsorbable, Synthetic, Polyamide |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-07-10 |
Device Publish Date | 2020-07-02 |
00812444029031 | Suture |
10812444029021 | Suture |
10812444029014 | Suture |
00812444029000 | Suture |
10812444026235 | Suture |
10812444024538 | SUTURE |
10812444024521 | Suture |
10812444024484 | SUTURE |
10812444024477 | SUTURE |
10812444024460 | SUTURE |
00812444022896 | SUTURE |
00812444022889 | SUTURE |
10812444022879 | SUTURE |
10812444022862 | SUTURE |
10812444022855 | SUTURE |
10812444022848 | SUTURE |
10812444022831 | SUTURE |
10812444020103 | SUTURE |
00810020084108 | Suture |
10810020084099 | Suture |