Monofilament Polypropylene Synthetic non-absorbable Surgical Sututres / Ligatures
Who Else Makes It
Concentrated in Shandong (2), Beijing (1).
Record
Regulatory record for Unipro | Listed by | United Medical Industries Co., Ltd., Saudi Arabia |
| FDA product code | GAW |
| Device type | Suture, Nonabsorbable, Synthetic, Polypropylene |
| Device class | Class 2 |
| Regulation | 21 CFR 878.5010 |
| Establishment | Manufacturer |
| 510(k) | K042283 |
| Record published | 2020-04-30 |
| Record revised | 2023-06-02 (version 3) |
Specifications
Specifications | MRI safety | Labeling does not contain MRI Safety Information |
| Supplied sterile | Yes |
| Single use | Yes |
| Latex | Labelled latex-free |
| Label carries | lot or batch number, expiry date, serial number |
| Storage | Storage environment temperature up to 25 °C; Handling environment temperature up to 25 °C |
| Sizes | Outer diameter 0.3 mm |
PMA Approvals
A premarket approval is the full Class III route, granted on clinical evidence rather than on equivalence to an existing device. It is the highest regulatory bar a device of this type can clear.
Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.