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Plasma Control 0236

by Chromsystems Instruments & Chemicals GmbH

Plasma Control 0236 is a Class I device made by Chromsystems Instruments & Chemicals GmbH, listed in FDA GUDID since 30 Jul 2020 (UDI-DI 04250317544537), 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 Number04250317544537 UDI-DI Date30 Jul 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  • Withdrawn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
Mycophenolate therapeutic drug monitoring IVD, control
Model / Ref / Catalog
0236
Primary DI / UDI-DI
04250317544537
FDA product code
LAS
GMDN term
Mycophenolate therapeutic drug monitoring IVD, control
Device class
Class I
Regulation number
862.3280
GUDID distribution status
In Commercial Distribution

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)