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Alfa Wassermann

FDA UDI

Class II (US FDA UDI)

by Alfa Wassermann, Inc.

Identity

Trade Name
Alfa Wassermann FDA UDI
Generic Name
Multiple-type clinical chemistry analyte profile IVD, calibrator FDA UDI
Device Name
Urine Standard FDA UDI
Model / Reference
S2-85 FDA UDI
Description
Urine Standard FDA UDI

Identifiers

Catalog Number
S2-85 FDA UDI
Primary DI / UDI-DI
00857969006198 FDA UDI
FDA Product Code
JIX FDA UDI
GMDN Term
Multiple-type clinical chemistry analyte profile IVD, calibrator FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.1150 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

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

Category: Multiple-type clinical chemistry analyte profile IVD, calibrator

Alfa Wassermann by Alfa Wassermann, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Multiple-type clinical chemistry analyte profile IVD, calibrator.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 81179f4c-2fb6-4641-b4f8-445b8fde8d28 36 fields · synced Jun 8, 2026