Remy Zft-15FJ
by Wuhan Dimed Laser Technology Co., Ltd.
Remy Zft-15FJ is a Class II device made by Wuhan Dimed Laser Technology Co., Ltd., listed in FDA GUDID since 14 Oct 2025 (UDI-DI 06974214160789), 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 | Number06974214160789 | Date14 Oct 2025 | StatusListed |
Official records
- AccessGUDID record 06974214160789
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Remy
- Generic name
- Musculoskeletal/physical therapy laser, professional
- Model / reference
- ZFT-15FJ
- Primary DI / UDI-DI
- 06974214160789
- FDA product code
- ILY, GEX, PDZ
- GMDN term
- Musculoskeletal/physical therapy laser, professional
- Device class
- Class II
- Regulation number
- 890.5500, 878.4810
- GUDID distribution status
- In Commercial Distribution
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