Identity
- Trade Name
- C3 FDA UDI
- Generic Name
- Complement component C3 proactivator IVD, reagent FDA UDI
- Device Name
- A Complement C3 test system is a device intended for the quantitative in vitro determination of Complement C3 concentration in serum FDA UDI
- Model / Reference
- CM3845 FDA UDI
- Description
- A Complement C3 test system is a device intended for the quantitative in vitro determination of Complement C3 concentration in serum FDA UDI
Identifiers
- Catalog Number
- CM3845 FDA UDI
- Primary DI / UDI-DI
- 05055273201611 FDA UDI
- FDA Product Code
- CZW FDA UDI
- GMDN Term
- Complement component C3 proactivator IVD, reagent FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 866.5240 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
Yes
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Complement component C3 proactivator IVD, reagent
C3 by Randox Laboratories, Ltd. — 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
- Randox Laboratories, Ltd.
Sources (1)
- FDA UDI 6bf3d0b2-abda-41f4-8d53-90749f910ed7 36 fields · synced May 30, 2026