Primary Device ID | 00812444021035 |
NIH Device Record Key | f51a32e9-be6d-4ce9-842e-7345fffe2050 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | PDM |
Version Model Number | D451 |
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 | false |
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 | 00812444021035 [Primary] |
GS1 | 10812444021032 [Package] Package: [12 Units] In Commercial Distribution |
NEW | Suture, Surgical, Absorbable, Polydioxanone |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2019-02-07 |
Device Publish Date | 2015-10-16 |
00812444021103 | SUTURE |
00812444021097 | SUTURE |
00812444021080 | SUTURE |
00812444021073 | SUTURE |
00812444021066 | SUTURE |
00812444021059 | SUTURE |
00812444021042 | SUTURE |
00812444021035 | SUTURE |
00812444021011 | SUTURE |
00812444021004 | SUTURE |
00812444020991 | SUTURE |
00812444020984 | SUTURE |
00812444020977 | SUTURE |
00812444020960 | SUTURE |
00812444020953 | SUTURE |
00812444020946 | SUTURE |
00812444020939 | SUTURE |
00812444020922 | SUTURE |
00812444020915 | SUTURE |
00812444020908 | SUTURE |
00812444020892 | SUTURE |
00812444020885 | SUTURE |
10812444029298 | Suture |
10812444021025 | Suture |
10810020084723 | Suture |
10810020084716 | Suture |
10810020084709 | Suture |
10810020084693 | Suture |