Identity
- Trade Name
- 800,102 P37,R4,BE,2L,STKR FDA UDI
- Generic Name
- Electrical mains power extension cable FDA UDI
- Device Name
- 800,102 P37,R4,BE,2L,STKR FDA UDI
- Model / Reference
- IC-0856 FDA UDI
- Description
- 800,102 P37,R4,BE,2L,STKR FDA UDI
Identifiers
- Catalog Number
- 7807 FDA UDI
- Primary DI / UDI-DI
- 00840828157551 FDA UDI
- FDA Product Code
- ILQ FDA UDI
- GMDN Term
- Electrical mains power extension cable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 890.3710 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
Yes
FDA UDI
800, 102 P37, R4, Be, 2l, Stkr by Curbell Medical Products, Inc. — 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
- Curbell Medical Products, Inc.
Sources (1)
- FDA UDI cf07c0b1-7d55-4bf3-9e54-8f40e49cee1a 36 fields · synced Jun 1, 2026