Identity
- Trade Name
- Lumipulse G B-Amyloid Controls (Plasma)-N FDA UDI
- Generic Name
- Tau protein IVD, kit, chemiluminescent immunoassay FDA UDI
- Device Name
- Lumipulse G B-Amyloid Controls (Plasma)-N FDA UDI
- Model / Reference
- 235485 FDA UDI
- Description
- Lumipulse G B-Amyloid Controls (Plasma)-N FDA UDI
Identifiers
- Primary DI / UDI-DI
- 04987270235485 FDA UDI
- GMDN Term
- Tau protein IVD, kit, chemiluminescent immunoassay FDA UDI
Classification
- 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
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
Lumipulse G B-Amyloid Controls (Plasma)-N by Fujirebio Inc. — 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 | N/A | Pending data |
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Manufacturer
- Manufacturer
- Fujirebio Inc.
Sources (1)
- FDA UDI 130df900-b2b6-421c-9b1d-922abcec70ec 37 fields · synced May 29, 2026