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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 electrolyte IVD, calibrator FDA UDI
Device Name
CAL A FDA UDI
Model / Reference
SA1029 FDA UDI
Description
CAL A FDA UDI

Identifiers

Catalog Number
SA1029 FDA UDI
Primary DI / UDI-DI
00857969006389 FDA UDI
FDA Product Code
JIX FDA UDI
GMDN Term
Multiple electrolyte 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 electrolyte 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 electrolyte IVD, calibrator.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI f70a581b-dbda-4e2e-a0ad-ca47cf717eae 36 fields · synced May 30, 2026