Avance 7703014-00
by Talley Group, Ltd. GUDID
Withdrawn
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number07323190130870 | Date24 Sep 2016 | StatusWithdrawn |
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not known
- Not covered
United States — GUDID listing Listed
Recalls
No FDA recalls on record, checked 22 Oct 2026.
Specification
- Trade Name
- Avance
- Generic Name
- Negative-pressure wound therapy system, battery-powered, reusable
- Model / Ref / Catalog
- 7703014-00, 7703014
- Primary DI / UDI-DI
- 07323190130870
- FDA Product Code
- OMP
- GMDN Term
- Negative-pressure wound therapy system, battery-powered, reusable
- Device Class
- Class II
- Regulation Number
- 878.4780
- Commercial Distribution
- Not in Commercial Distribution
Other devices from Talley Group, Ltd.
Properties
Other properties (12)
- Sterile: No
- Single Use: No
- Implantable: No
- Contains Latex: No
- Prescription Use: No
- Over-the-Counter: No
- Convenience Kit: No
- Combination Product: No
- HCT/P: No
- Premarket Exempt: No
- Expiration Date: No
- Manufacturing Date: No