| Primary Device ID | 00812444020144 |
| NIH Device Record Key | d37c15c2-6519-46da-9724-c699c8d7d03d |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | SURGIPOINT |
| Version Model Number | VGQ392 |
| 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 | 00812444020144 [Primary] |
| GS1 | 10812444020141 [Package] Package: [12 Units] In Commercial Distribution |
| GAM | Suture, Absorbable, Synthetic, Polyglycolic Acid |
| 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 | 2015-10-22 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() SURGIPOINT 85798651 4433870 Live/Registered |
Salvin Dental Specialties, Inc. 2012-12-10 |