PADnet Xpress 1.0
by Collaborative Care Diagnostics LLC
PADnet Xpress 1.0 is a Class II device made by Collaborative Care Diagnostics LLC, listed in FDA GUDID since 4 Feb 2026 (UDI-DI 00862467000333), 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 | Number00862467000333 | Date4 Feb 2026 | StatusListed |
Official records
- AccessGUDID record 00862467000333
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- PADnet Xpress
- Generic name
- Limb plethysmograph
- Model / reference
- 1.0
- Primary DI / UDI-DI
- 00862467000333
- FDA product code
- JOM
- GMDN term
- Limb plethysmograph
- Device class
- Class II
- Regulation number
- 870.2780
- GUDID distribution status
- In Commercial Distribution
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