N/A 1057801
by George Tiemann & Co. United States GUDID
Product code HTF
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | NumberB58210578010 | Date24 Sep 2020 | StatusIn distribution |
Coverage
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade Name
- N/A
- Generic Name
- Dermal curette, single-use
- Model / Ref / Catalog
- 1057801
- Primary DI / UDI-DI
- B58210578010
- FDA Product Code
- HTF
- GMDN Term
- Dermal curette, single-use
- Device Class
- Class I
- Regulation Number
- 878.4800
- Commercial Distribution
- In Commercial Distribution
Other devices from George Tiemann & Co.
Properties & raw data
Show properties, registry sources and raw records
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
- Serial Number: No
- Expiration Date: No
- Manufacturing Date: No
Sources (1)
- FDA UDI 25f9b6a5-1a79-4d65-96bc-25372a4f8775