| Primary Device ID | 10810020085997 |
| NIH Device Record Key | 779e51a7-cd51-4301-a1a8-508748fd4c27 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | PowerSuture Tape |
| Version Model Number | 05.03.0194 |
| 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 | 00810020085990 [Primary] |
| GS1 | 10810020085997 [Package] Contains: 00810020085990 Package: [10 Units] In Commercial Distribution |
| GAT | Suture, Nonabsorbable, Synthetic, Polyethylene |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2024-05-20 |
| Device Publish Date | 2024-05-10 |
| 10810020084532 | Suture |
| 10810020084525 | Suture |
| 10810020084518 | Suture |
| 10810020084471 | Suture |
| 10810020084464 | Suture |
| 10810020084457 | Suture |
| 10810020084440 | Suture |
| 10810020084433 | Suture |
| 10810020084426 | Suture |
| 10810020084419 | Suture |
| 10810020084402 | Suture |
| 10840277404395 | Meniscal Needles – Double Armed, Black Braided UHMWPE Non-Absorbable Suture |
| 10840277404388 | Meniscal Needles – Single Armed, Black Braided UHMWPE Non-Absorbable Suture |
| 10840277404364 | Meniscal Needles – Single Armed Blue Braided UHMWPE Non-Absorbable Suture |
| 10810020085997 | Meniscal Needles – Double Armed, Blue Braided UHMWPE Non-Absorbable Suture Tape |