2 catalogue numbers from 9E70DZ26, listed by Healthium Medtech Limited, India, under Suture, Surgical, Absorbable, Polydioxanone. 2 manufacturers in China are registered for this product code.
Who Else Makes It
Concentrated in Shandong (1), Beijing (1).
Record
Regulatory record for PD Synth | Listed by | Healthium Medtech Limited, India |
| FDA product code | NEW |
| Device type | Suture, Surgical, Absorbable, Polydioxanone |
| Device class | Class 2 |
| Regulation | 21 CFR 878.4840 |
| Establishment | Specification developer, Manufacturer |
| Record published | 2025-02-16 |
Specifications
Specifications | MRI safety | Labeling does not contain MRI Safety Information |
| Supplied sterile | Yes |
| Single use | Yes |
| Label carries | lot or batch number, expiry date, manufacturing date |
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.