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Alfa Wassermann

FDA UDI

by Alfa Wassermann, Inc.

Identity

Trade Name
Alfa Wassermann FDA UDI
Generic Name
Ion selective electrode (ISE) reference solution IVD, reagent FDA UDI
Device Name
STARLYTE V Fluid Pack FDA UDI
Model / Reference
E1-9 FDA UDI
Description
STARLYTE V Fluid Pack FDA UDI

Identifiers

Catalog Number
E1-9 FDA UDI
Primary DI / UDI-DI
00857969006372 FDA UDI
GMDN Term
Ion selective electrode (ISE) reference solution IVD, reagent FDA UDI

Classification

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, calibratorIon selective electrode (ISE) reference solution IVD, reagent

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

Similar devices

Also classified as Ion selective electrode (ISE) reference solution IVD, reagent.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI f754baaf-2a2d-4ffb-b1d1-7403e0716362 36 fields · synced Jun 6, 2026