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Elecsys beta-Amyloid (1-42) CSF II

FDA UDI

Class II (US FDA UDI)

by Roche Diagnostics Corp.

Identity

Trade Name
Elecsys beta-Amyloid (1-42) CSF II FDA UDI
Generic Name
Amyloid B component IVD, kit, chemiluminescent immunoassay FDA UDI
Model / Reference
08821941190 FDA UDI

Identifiers

Catalog Number
08821941190 FDA UDI
Primary DI / UDI-DI
07613336166321 FDA UDI
510(k) Number
K221842 FDA UDI
K231348 FDA UDI
FDA Product Code
QSE FDA UDI
GMDN Term
Amyloid B component IVD, kit, chemiluminescent immunoassay FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
866.5840 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

No

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: Amyloid B component IVD, kit, chemiluminescent immunoassay

Elecsys beta-Amyloid (1-42) CSF II by Roche Diagnostics Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Amyloid B component IVD, kit, chemiluminescent immunoassay.

Cleared under the same submission

K221842 also covers:

K231348 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Roche Diagnostics Corp.

Sources (1)

  • FDA UDI f97d8946-9c68-4f30-b2fe-072d687816b6 34 fields · synced May 30, 2026