Identity
- Trade Name
- Lumipulse Infectious Disease Controls FDA UDI
- Generic Name
- Multiple blood-borne virus antigen/antibody IVD, control FDA UDI
- Model / Reference
- 235584 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 04987270235584 FDA UDI
- FDA Product Code
- OHQ FDA UDI
- GMDN Term
- Multiple blood-borne virus antigen/antibody IVD, control FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 862.1660 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
Yes
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
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Multiple blood-borne virus antigen/antibody IVD, control
Lumipulse Infectious Disease Controls by Fujirebio Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Multiple blood-borne virus antigen/antibody IVD, control.
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- VIROTROL — Bio-Rad Laboratories · Class II
- VIROTROL — Bio-Rad Laboratories · Class II
- VIROTROL — Bio-Rad Laboratories · Class II
- VIROTROL — Bio-Rad Laboratories · Class II
- VIROCLEAR — Bio-Rad Laboratories · Class II
- VIROTROL — Bio-Rad Laboratories · 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 I | Pending data |
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Manufacturer
- Manufacturer
- Fujirebio Inc.
Sources (1)
- FDA UDI df5013da-09f7-4a4b-8dbb-75fbc41209bf 35 fields · synced May 30, 2026