Digital Portable Ems Dgems
by Dynatronics Corp. 2 variants
Digital Portable Ems Dgems is a Class II device made by Dynatronics Corp., listed in FDA GUDID since 18 Oct 2018 (UDI-DI 10660584000420), not in commercial distribution (GUDID) 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 | Number10660584000420 | Date18 Oct 2018 | StatusListed |
Official records
- AccessGUDID record 10660584000420
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Digital Portable Ems
- Generic name
- Physical therapy transcutaneous neuromuscular electrical stimulation system
- Model / reference
- DGEMS
- Primary DI / UDI-DI
- 10660584000420
- FDA product code
- IPF, GZJ
- GMDN term
- Physical therapy transcutaneous neuromuscular electrical stimulation system
- Device class
- Class II
- Regulation number
- 890.5850, 882.5890
- GUDID distribution status
- Not in Commercial Distribution
- Size
- Width — 61.5 MillimeterLength — 108 MillimeterHeight — 25.0 Millimeter
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