TheraTouch UX2 DQ2000
TheraTouch UX2 DQ2000 is a Class II device made by Drive Devilbiss Healthcare, listed in FDA GUDID since 7 Sep 2022 (UDI-DI 00092237623817), 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 | Number00092237623817 | Date7 Sep 2022 | StatusListed |
Official records
- AccessGUDID record 00092237623817
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- TheraTouch UX2
- Generic name
- Analgesic transcutaneous electrical nerve stimulation system
- Model / reference
- DQ2000
- Primary DI / UDI-DI
- 00092237623817
- FDA product code
- GZJ, HCC, IPF, LIH, IMG, GZI
- GMDN term
- Analgesic transcutaneous electrical nerve stimulation system
- Device class
- Class II
- Regulation number
- 882.5890, 882.5050, 890.5850, 890.5860, 882.5810
- GUDID distribution status
- In Commercial Distribution
- MRI safety
- MR Safe
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