| Primary Device ID | 20884521047447 |
| NIH Device Record Key | a6142e07-5ee6-49b4-a994-f882a79054ed |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | TA 90 B |
| Version Model Number | 015888L |
| Catalog Number | 015888L |
| Company DUNS | 058614483 |
| Company Name | Covidien LP |
| 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 | true |
| OTC Over-The-Counter | false |
| Phone | +1(508)261-8000 |
| covidien.udi@covidien.com |
| Height | 4.8 Millimeter |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 10884521047440 [Primary] |
| GS1 | 20884521047447 [Package] Contains: 10884521047440 Package: CASE [6 Units] In Commercial Distribution |
| GDW | STAPLE, IMPLANTABLE |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 5 |
| Public Version Date | 2019-05-07 |
| Device Publish Date | 2015-08-28 |
| 10884521744134 - TruClear | 2024-04-23 Calibration Insert |
| 10884521744141 - TruClear | 2024-04-23 Calibration Insert |
| 10884521557048 - INVOS | 2024-04-22 Docking Station |
| 10884521833869 - Endoflip | 2024-04-22 Refurbished 300 Pump System With Pre-Use Tube |
| 20884521140216 - ClosureFast | 2024-04-15 Compression Bandages,Cohesive,6"" x 15' (15.24 cm x 4.572 m) |
| 10884521543430 - LiquiBand Exceed | 2024-04-15 2-Octyl Cyanoacrylate |
| 20884521140209 - ClosureFast | 2024-04-10 Compression Bandages,Cohesive,4"" x 15' (10.16 cm x 4.572 m) |
| 10884521539921 - VenaSeal | 2024-04-09 VenaSeal Closure System |