BOSS Instruments 80-2402
BOSS Instruments 80-2402 is a Class I device made by Boss Instruments, Ltd., listed in FDA GUDID since 28 Feb 2024 (UDI-DI 00888515209787), 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 | Number00888515209787 | Date28 Feb 2024 | StatusListed |
Official records
- AccessGUDID record 00888515209787
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- BOSS Instruments
- Generic name
- Ophthalmic calliper
- Model / Ref / Catalog
- 80-2402
- Primary DI / UDI-DI
- 00888515209787
- FDA product code
- HOE
- GMDN term
- Ophthalmic calliper
- Device class
- Class I
- Regulation number
- 886.4350
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
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