Identity
- Trade Name
- The Freedom Bed FDA UDI
- Generic Name
- Kinetic bed FDA UDI
- Device Name
- Base model – rotation only FDA UDI
- Model / Reference
- PAR3-A2 FDA UDI
- Description
- Base model – rotation only FDA UDI
Identifiers
- Primary DI / UDI-DI
- B414PAR3A20 FDA UDI
- FDA Product Code
- IKZ FDA UDI
- GMDN Term
- Kinetic bed FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 890.5225 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
Yes
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
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Kinetic bed
The Freedom Bed by Probed Medical Technologies, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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- Multicare — L I N E T spol. s r.o. · Class II
- Multicare — L I N E T spol. s r.o. · Class II
- Multicare — L I N E T spol. s r.o. · 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 II | Pending data |
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Manufacturer
- Manufacturer
- Probed Medical Technologies, Inc.
Sources (1)
- FDA UDI 1259b88f-1079-49de-acb1-cec9b8a47944 34 fields · synced Jun 8, 2026