Omnia Medical Instruments 99-5A-CPP1
Omnia Medical Instruments 99-5A-CPP1 is a Class I device made by Omnia Medical, listed in FDA GUDID since 15 Jul 2025 (UDI-DI 00843511128258), registry data as of 22 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 | Number00843511128258 | Date15 Jul 2025 | StatusListed |
Official records
- AccessGUDID record 00843511128258
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Omnia Medical Instruments
- Generic name
- Bone access cannula
- Model / Ref / Catalog
- 99-5A-CPP1
- Primary DI / UDI-DI
- 00843511128258
- FDA product code
- HXB
- GMDN term
- Bone access cannula
- Device class
- Class I
- Regulation number
- 888.4540
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
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