DermaFuse DER0110
by Viora Ltd
DermaFuse DER0110 is a Class I device made by Viora Ltd, listed in FDA GUDID since 21 May 2025 (UDI-DI 07290016746495), 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 | Number07290016746495 | Date21 May 2025 | StatusListed |
Official records
- AccessGUDID record 07290016746495
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- DermaFuse
- Generic name
- Transcutaneous electrical stimulation lead
- Model / Ref / Catalog
- DER0110
- Primary DI / UDI-DI
- 07290016746495
- FDA product code
- ISA
- GMDN term
- Transcutaneous electrical stimulation lead
- Device class
- Class I
- Regulation number
- 890.5660
- GUDID distribution status
- In Commercial Distribution
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