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CytoCell myProbes MPP6952

by Cytocell, Ltd. 2 variants

CytoCell myProbes MPP6952 is a Class I device made by Cytocell, Ltd., listed in FDA GUDID since 2 Sep 2026 (UDI-DI 05055844936768), 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 Number05055844936768 UDI-DI Date2 Sep 2026ListedStatusListed 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  • Withdrawn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
CytoCell myProbes
Generic name
Assay development analyte-specific reagent IVD
Model / reference
MPP6952
Primary DI / UDI-DI
05055844936768
FDA product code
MVU
GMDN term
Assay development analyte-specific reagent IVD
Device class
Class I
Regulation number
864.4020
GUDID distribution status
In Commercial Distribution

Other devices from Cytocell, Ltd.

See all devices from Cytocell, Ltd. →

Properties

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