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Validate 1100ab

by LGC Clinical Diagnostics, Inc.

Validate 1100ab is a Class I device made by LGC Clinical Diagnostics, Inc., listed in FDA GUDID since 19 Oct 2018 (UDI-DI 00859110005180), 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 Number00859110005180 UDI-DI Date19 Oct 2018ListedStatusListed 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  • Withdrawn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
Validate
Generic name
Multiple-type clinical chemistry analyte profile IVD, control
Model / Ref / Catalog
1100ab
Primary DI / UDI-DI
00859110005180
FDA product code
JJY
GMDN term
Multiple-type clinical chemistry analyte profile IVD, control
Device class
Class I
Regulation number
862.1660
GUDID distribution status
In Commercial Distribution

Related devices

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

Similar devices in this category

Other devices filed under Multiple-type clinical chemistry analyte profile IVD, control.

Other devices from LGC Clinical Diagnostics, Inc.

See all devices from LGC Clinical Diagnostics, Inc. →

Properties

  • Single use
  • Prescription use
  • Convenience kit
  • Lot / batch number
  • Expiration date
Other properties (10, all answered No)