CytoCell myProbes MPD51562

by Cytocell, Ltd.

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

Registry data, not yet checked by deviCERTS. Source GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number05055844935693 UDI-DI	Date20 Apr 2026Listed	StatusListed GUDID: in commercial distribution

Official records

AccessGUDID record UDI-DI 05055844935693

Coverage

1 jurisdiction

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Withdrawn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: MPD51562

Primary DI / UDI-DI: 05055844935693
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

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Properties

Premarket exempt
Lot / batch number
Manufacturing date

Other properties (12)

Supplied sterile: No
Sterilise before use: No
Single use: No
Implantable: No
Contains latex: No
Prescription use: No
Over-the-counter: No
Convenience kit: No
Combination product: No
HCT/P: No
Serial number: No
Expiration date: No