Epimed 301-1815
Epimed 301-1815 is a Class II device made by Epimed International, Inc, listed in FDA GUDID since 26 Aug 2020 (UDI-DI 00818788023483), 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 | Number00818788023483 | Date26 Aug 2020 | StatusListed |
Official records
- AccessGUDID record 00818788023483
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Epimed
- Generic name
- Percutaneous radio-frequency ablation probe, denervation, monopolar, single-use
- Model / Ref / Catalog
- 301-1815
- Primary DI / UDI-DI
- 00818788023483
- FDA product code
- GXI
- GMDN term
- Percutaneous radio-frequency ablation probe, denervation, monopolar, single-use
- Device class
- Class II
- Regulation number
- 882.4725
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Ethylene Oxide
- MRI safety
- MR Unsafe
- Size
- Needle Gauge — 18 GaugeLength — 15 CentimeterLength — 10 Millimeter
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