Ltj 81004162682
by Azurmeds, Inc. GUDID
Withdrawn
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00810041626820 | Date16 Jan 2022 | 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- Withdrawn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
- Ltj
- Generic Name
- Hand-held surgical retractor, reusable
- Model / Reference
- 81004162682
- Primary DI / UDI-DI
- 00810041626820
- FDA Product Code
- GAD
- GMDN Term
- Hand-held surgical retractor, reusable
- Device Class
- Class I
- Regulation Number
- 878.4800
- Commercial Distribution
- Not in Commercial Distribution
- Sterilization Method
- Moist Heat or Steam Sterilization
Other devices from Azurmeds, Inc.
Properties
Other properties (10)
- Sterile: No
- Single Use: No
- Implantable: No
- Contains Latex: No
- Over-the-Counter: No
- Convenience Kit: No
- Combination Product: No
- HCT/P: No
- Serial Number: No
- Expiration Date: No