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Plasma Control 0133

by Chromsystems Instruments & Chemicals GmbH

Plasma Control 0133 is a medical device (FDA Class I; FDA product code LAS, Drug Specific Control Materials) made by Chromsystems Instruments & Chemicals GmbH, listed in FDA GUDID since 27 Aug 2020 (UDI-DI 04250317544339), registry data as of 23 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number04250317544339 UDI-DI Date27 Aug 2020ListedStatusListed 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  • Withdrawn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
Plasma Control
Generic name
Multiple antipsychotic therapeutic drug monitoring IVD, control
Model / Ref / Catalog
0133
Primary DI / UDI-DI
04250317544339
FDA product code
LAS
GMDN term
Multiple antipsychotic therapeutic drug monitoring IVD, control
Device class
Class I
Regulation number
862.3280
GUDID distribution status
In Commercial Distribution

Related devices

Category: Multiple antipsychotic therapeutic drug monitoring IVD, control

Similar devices

Other devices filed under FDA product code LAS (Drug Specific Control Materials).

Other devices from Chromsystems Instruments & Chemicals GmbH

See all devices from Chromsystems Instruments & Chemicals GmbH →

Properties

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