Identity
- Trade Name
- TIDI FDA UDI
- Generic Name
- Multifunction body cushion FDA UDI
- Device Name
- HEAD REST, CERVICAL FDA UDI
- Model / Reference
- 733-BLUE FDA UDI
- Description
- HEAD REST, CERVICAL FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00618125177202 FDA UDI
- FDA Product Code
- IWY FDA UDI
- GMDN Term
- Multifunction body cushion FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 892.1920 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
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
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Tidi by Tidi Products, Llc — Class I — 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 I | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Tidi Products, Llc
Sources (1)
- FDA UDI 1e987f9c-2ea6-4f14-b388-c8e14e4eb4c2 34 fields · synced May 31, 2026