Cannula Standard
by Alpha Omega Engineering Corp. 30 variants
Cannula Standard (366-019921-00) is a Class II device made by Alpha Omega Engineering Corp., listed in FDA GUDID since 24 Sep 2016 (UDI-DI 07290016450682), 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 | Number07290016450682 | Date24 Sep 2016 | StatusListed |
Official records
- AccessGUDID record 07290016450682
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Cannula
- Generic name
- Intracerebral cannula, implantable
- Model / Ref / Catalog
- Standard, 366-019921-00
- Primary DI / UDI-DI
- 07290016450682
- FDA product code
- GZL
- GMDN term
- Intracerebral cannula, implantable
- Device class
- Class II
- Regulation number
- 882.1330
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
- MRI safety
- MR Unsafe
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