Primary Device ID | 10812444028932 |
NIH Device Record Key | 4e9e4631-6fe4-4659-a393-ffdcdbcb42fc |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | CuffTape |
Version Model Number | HS213 |
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 | 00812444028935 [Primary] |
GS1 | 10812444028932 [Package] Contains: 00812444028935 Package: [6 Units] In Commercial Distribution |
GAT | Suture, Nonabsorbable, Synthetic, Polyethylene |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2020-01-29 |
Device Publish Date | 2018-11-27 |
10812444028932 | Suture |
10812444027188 | Suture |
10812444027171 | Suture |
00810020082913 | suture |
10810020085058 | Suture |
10810020085041 | Suture |
10810020081883 | Suture |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
CUFFTAPE 88207209 5893440 Live/Registered |
TIGON MEDICAL 2018-11-27 |
CUFFTAPE 87603031 not registered Dead/Abandoned |
Tigon Medical 2017-09-11 |