Microtek 1
by Microtek Medical LLC 1,000+ variants
Microtek 1 is a Class II device made by Microtek Medical LLC, listed in FDA GUDID since 6 Jan 2017 (UDI-DI 00748426119783), registry data as of 23 Oct 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00748426119783 | Date6 Jan 2017 | StatusListed |
Official records
- AccessGUDID record 00748426119783
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Microtek
- Generic name
- C-arm drape
- Model / reference
- 1
- Primary DI / UDI-DI
- 00748426119783
- FDA product code
- KKX
- GMDN term
- C-arm drape
- Device class
- Class II
- Regulation number
- 878.4370
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Ethylene Oxide
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