GII SNAP-PAK SNAP-PAK Size 2 (5 metric) green ETHIBOND braided polyester suture, 36 Inches (91cm), double-armed with CP-2 needles
Who Else Makes It
Registered in Shanghai.
Record
Regulatory record for GII Ethibond | Listed by | DePuy Mitek, Inc., United States |
| FDA product code | GAS |
| Device type | Suture, Nonabsorbable, Synthetic, Polyester |
| Device class | Class 2 |
| Regulation | 21 CFR 878.5000 |
| Establishment | Specification developer, Manufacturer |
| Premarket notification | Exempt |
| Record published | 2015-09-01 |
| Record revised | 2021-09-27 (version 6) |
Specifications
Specifications | MRI safety | MR Conditional |
| Supplied sterile | Yes |
| Single use | Yes |
| Prescription | Prescription only |
| Label carries | lot or batch number, expiry date |
| Storage | Storage environment temperature up to 77 °F; Storage environment temperature up to 25 °C; Handling environment temperature up to 77 °F; Handling environment temperature up to 25 °C |
| Packaging | Package of 5 |
| Distribution end date | 2021-01-28 |
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.