BOSS Instruments 93-1737
BOSS Instruments 93-1737 is a Class I device made by Boss Instruments, Ltd., listed in FDA GUDID since 28 Feb 2024 (UDI-DI 00888515241923), 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 | Number00888515241923 | Date28 Feb 2024 | StatusListed |
Official records
- AccessGUDID record 00888515241923
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- BOSS Instruments
- Generic name
- Nasal speculum, reusable
- Model / Ref / Catalog
- 93-1737
- Primary DI / UDI-DI
- 00888515241923
- FDA product code
- EPY
- GMDN term
- Nasal speculum, reusable
- Device class
- Class I
- Regulation number
- 878.1800
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
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