Identity
- Trade Name
- CHATTANOOGA FDA UDI
- Generic Name
- Continuous passive motion joint exerciser FDA UDI
- Device Name
- KIT SFTGOODS ARTRMOT S2 PROARM FDA UDI
- Model / Reference
- 20719 FDA UDI
- Description
- KIT SFTGOODS ARTRMOT S2 PROARM FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00888912268806 FDA UDI
- FDA Product Code
- ILZ FDA UDI
- GMDN Term
- Continuous passive motion joint exerciser FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 890.5925 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
Yes
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Continuous passive motion joint exerciser
Chattanooga by Djo, Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Continuous passive motion joint exerciser.
- rebless — H ROBOTICS INC. · Class I
- OmniCycle Connect — medica Medizintechnik GmbH · Class I
- rebless — H ROBOTICS INC. · Class I
- EZ Stretch — FULL RANGE REHAB LLC · Class I
- rebless — H ROBOTICS INC. · Class I
- rebless — H ROBOTICS INC. · Class I
- rebless — H ROBOTICS INC. · Class I
- rebless (Model: RHDB) — H ROBOTICS INC. · Class II
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Djo, Llc
Sources (1)
- FDA UDI 87d31d6e-d10e-4e3a-af1e-e94d0fe0e6d6 33 fields · synced May 30, 2026