Primary Device ID | 10810020081869 |
NIH Device Record Key | 3f50dcc0-00c2-4a29-aa21-1f8ff722b3e7 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | SURGIPOINT |
Version Model Number | Q388 |
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 | 00810020081862 [Primary] |
GS1 | 10810020081869 [Package] Contains: 00810020081862 Package: [12 Units] In Commercial Distribution |
GAM | Suture, Absorbable, Synthetic, Polyglycolic Acid |
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 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() SURGIPOINT 85798651 4433870 Live/Registered |
Salvin Dental Specialties, Inc. 2012-12-10 |