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Alkaline Phosphatase 2115-0

by Sterling Diagnostics Inc

Alkaline Phosphatase 2115-0 is a device made by Sterling Diagnostics Inc, listed in FDA GUDID since 14 Sep 2016 (UDI-DI 00852223007140), registry data as of 22 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00852223007140 UDI-DI Date14 Sep 2016ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Alkaline Phosphatase
Generic name
Alkaline phosphatase (ALP) isoenzyme IVD, reagent
Model / Ref / Catalog
2115-0
Description
ALKALINE PHOSPHATASE (COLORIMETRIC TMP)
Primary DI / UDI-DI
00852223007140
GMDN term
Alkaline phosphatase (ALP) isoenzyme IVD, reagent
GUDID distribution status
In Commercial Distribution

Related devices

Category: Alkaline phosphatase (ALP) isoenzyme IVD, reagent

Other devices from Sterling Diagnostics Inc

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Properties

  • Convenience kit
  • Lot / batch number
  • Expiration date
Other properties (12, all answered No)