Pan system V5000

by Midmark Corporation

Pan system V5000 is a Class II device made by Midmark Corporation, listed in FDA GUDID since 22 Sep 2016 (UDI-DI 00841709102769), 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

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number00841709102769 UDI-DI	Date22 Sep 2016Listed	StatusListed GUDID: in commercial distribution

Official records

AccessGUDID record UDI-DI 00841709102769

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name: Pan system
Generic name: Stationary panoramic dental x-ray system, digital
Model / Ref / Catalog: V5000

Primary DI / UDI-DI: 00841709102769
FDA product code: MUH
GMDN term: Stationary panoramic dental x-ray system, digital

Device class: Class II
Regulation number: 872.1800
GUDID distribution status: In Commercial Distribution

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Properties

Prescription use
Serial number
Manufacturing date

Other properties (12, all answered No)