Primary Device ID | 10810020084624 |
NIH Device Record Key | 7230b71f-479d-49aa-96bd-27e1183b628b |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | CYTOSURG |
Version Model Number | T8664C |
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 | 00810020084627 [Primary] |
GS1 | 10810020084624 [Package] Contains: 00810020084627 Package: [12 Units] In Commercial Distribution |
NBY | Suture, Surgical, Nonabsorbable, Expanded, Polytetraflouroethylene |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-09-09 |
Device Publish Date | 2020-09-01 |
10812444020097 | SUTURE |
10812444020080 | SUTURE |
10812444020073 | SUTURE |
10812444020066 | SUTURE |
10812444020059 | SUTURE |
10812444020042 | SUTURE |
10812444020035 | SUTURE |
10812444020028 | SUTURE |
10812444020011 | SUTURE |
10810020084662 | Suture |
10810020084655 | Suture |
10810020084648 | Suture |
10810020084631 | Suture |
10810020084624 | Suture |
10810020084617 | Suture |
10810020084600 | Suture |
00810020084597 | Suture |
10810020084587 | Suture |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
CYTOSURG 87159559 5297981 Live/Registered |
Salvin Dental Specialties, Inc. 2016-09-02 |