Mjolnir Pro. LE-EPSMC
by Shenzhen Leaflife Technology Co., Ltd.
Mjolnir Pro. LE-EPSMC is an electrosurgical handpiece (FDA Class II; FDA product code QVJ, Low Power Electrosurgical Devices For Skin Lesion Destruction) made by Shenzhen Leaflife Technology Co., Ltd., listed in FDA GUDID since 9 Sep 2024 (UDI-DI 06974223650073), 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 | Number06974223650073 | Date9 Sep 2024 | StatusListed |
Official records
- AccessGUDID record 06974223650073
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Mjolnir Pro.
- Generic name
- Electrosurgical handpiece, single-use
- Model / reference
- LE-EPSMC
- Primary DI / UDI-DI
- 06974223650073
- FDA product code
- QVJ
- GMDN term
- Electrosurgical handpiece, single-use
- Device class
- Class II
- Regulation number
- 878.4400
- GUDID distribution status
- In Commercial Distribution
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