Precept® 22141
by Precept Medical Products, Inc.
Precept® 22141 is a Class I device made by Precept Medical Products, Inc., listed in FDA GUDID since 18 Sep 2018 (UDI-DI 10814707021964), 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 | Number10814707021964 | Date18 Sep 2018 | StatusListed |
Official records
- AccessGUDID record 10814707021964
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Precept®
- Generic name
- Surgical cap, single-use
- Model / reference
- 22141
- Primary DI / UDI-DI
- 10814707021964
- FDA product code
- FYF
- GMDN term
- Surgical cap, single-use
- Device class
- Class I
- Regulation number
- 878.4040
- GUDID distribution status
- In Commercial Distribution
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