Avanos MCKA3-17-150-4
Avanos MCKA3-17-150-4 is a Class II device made by Avanos Medical, Inc., listed in FDA GUDID since 11 Mar 2021 (UDI-DI 00193493000173), 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 | Number00193493000173 | Date11 Mar 2021 | StatusListed |
Official records
- AccessGUDID record 00193493000173
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Avanos
- Generic name
- Percutaneous radio-frequency ablation probe, denervation, bipolar
- Model / Ref / Catalog
- MCKA3-17-150-4
- Primary DI / UDI-DI
- 00193493000173
- FDA product code
- GXI
- GMDN term
- Percutaneous radio-frequency ablation probe, denervation, bipolar
- Device class
- Class II
- Regulation number
- 882.4725
- GUDID distribution status
- In Commercial Distribution
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