| Primary Device ID | 10840277402933 |
| NIH Device Record Key | dba312a1-d00e-4adc-9dbd-52ed90fe449d |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | SurgiPoint |
| Version Model Number | Q401 |
| Company DUNS | 964053560 |
| Company Name | RIVERPOINT MEDICAL, LLC |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | MR Safe |
| 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 | 00840277402936 [Primary] |
| GS1 | 10840277402933 [Package] Contains: 00840277402936 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 | 2023-12-13 |
| Device Publish Date | 2023-12-05 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() SURGIPOINT 85798651 4433870 Live/Registered |
Salvin Dental Specialties, Inc. 2012-12-10 |