Identity
- Trade Name
- Kobold FDA UDI
- Generic Name
- Multifunction body cushion FDA UDI
- Device Name
- Kobold Positioning Aid Kits 1in x 1in x 1in 1 per Each FDA UDI
- Model / Reference
- 32789 FDA UDI
- Description
- Kobold Positioning Aid Kits 1in x 1in x 1in 1 per Each FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00618125167418 FDA UDI
- FDA Product Code
- KXJ FDA UDI
- GMDN Term
- Multifunction body cushion FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 892.1980 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
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
No
FDA UDI
Kobold by Tidi Products, Llc — 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
- Tidi Products, Llc
Sources (1)
- FDA UDI 4fb9dc20-3155-44f7-b796-b4c6a1b33dbd 34 fields · synced Jun 1, 2026