Applicator MM01000-US
by Viora Ltd
Applicator MM01000-US is a Class II device made by Viora Ltd, listed in FDA GUDID since 22 May 2025 (UDI-DI 07290016746723), 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 | Number07290016746723 | Date22 May 2025 | StatusListed |
Official records
- AccessGUDID record 07290016746723
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Applicator
- Generic name
- Needleless medication/vaccine injector, pneumatic
- Model / Ref / Catalog
- MM01000-US
- Primary DI / UDI-DI
- 07290016746723
- FDA product code
- KZE
- GMDN term
- Needleless medication/vaccine injector, pneumatic
- Device class
- Class II
- Regulation number
- 880.5430
- GUDID distribution status
- In Commercial Distribution
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