Vitacore CAN99 9500
by Vitacore Industries, Inc. 2 variants
Vitacore CAN99 9500 is a Class II device made by Vitacore Industries, Inc., listed in FDA GUDID since 5 Sep 2024 (UDI-DI 00628678429024), 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 | Number00628678429024 | Date5 Sep 2024 | StatusListed |
Official records
- AccessGUDID record 00628678429024
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Vitacore
- Generic name
- Surgical/medical respirator, non-antimicrobial, single-use
- Model / reference
- CAN99 9500
- Primary DI / UDI-DI
- 00628678429024
- FDA product code
- MSH
- GMDN term
- Surgical/medical respirator, non-antimicrobial, single-use
- Device class
- Class II
- Regulation number
- 878.4040
- GUDID distribution status
- In Commercial Distribution
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