Identity
- Trade Name
- Hydrotherapy Whirlpool FDA UDI
- Generic Name
- Hydro-massage turbine FDA UDI
- Device Name
- MOBILE EXTREMITY WHIRLPOOL W/UK PWR CORD FDA UDI
- Model / Reference
- E-22-M-0003 FDA UDI
- Description
- MOBILE EXTREMITY WHIRLPOOL W/UK PWR CORD FDA UDI
Identifiers
- Catalog Number
- E-22-M-0009 FDA UDI
- Primary DI / UDI-DI
- 00645724002284 FDA UDI
- FDA Product Code
- ILJ FDA UDI
- GMDN Term
- Hydro-massage turbine FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 890.5100 FDA UDI
- Commercial Distribution
- Not 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
Yes
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
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Hydrotherapy Whirlpool by Whitehall Manufacturing Co — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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 II | Pending data |
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Manufacturer
- Manufacturer
- Whitehall Manufacturing Co
Sources (1)
- FDA UDI d49500b8-8846-4915-adf7-8a9e12a0b029 36 fields · synced May 30, 2026