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Diazyme DZ136A-K

by Diazyme Laboratories, Inc.

Diazyme DZ136A-K is a device made by Diazyme Laboratories, Inc., listed in FDA GUDID since 3 Nov 2016 (UDI-DI 00817089020207), 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 Number00817089020207 UDI-DI Date3 Nov 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  • Withdrawn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
Diazyme
Generic name
Albumin IVD, kit, spectrophotometry
Model / reference
DZ136A-K
Primary DI / UDI-DI
00817089020207
GMDN term
Albumin IVD, kit, spectrophotometry
GUDID distribution status
In Commercial Distribution

Related devices

Category: Albumin IVD, kit, spectrophotometry

Other devices from Diazyme Laboratories, Inc.

See all devices from Diazyme Laboratories, Inc. →

Properties

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