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Meicet M-906

by Shanghai May Skin Information Technology Co., Ltd.

Meicet M-906 is a Class II device made by Shanghai May Skin Information Technology Co., Ltd., listed in FDA GUDID since 27 Feb 2023 (UDI-DI 06975980572509), 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 Number06975980572509 UDI-DI Date27 Feb 2023ListedStatusListed 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  • Withdrawn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
Meicet
Generic name
Dermatoscope, digital
Model / reference
M-906
Primary DI / UDI-DI
06975980572509
FDA product code
PUH
GMDN term
Dermatoscope, digital
Device class
Class II
Regulation number
870.2770
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code PUH (Analyzer, Body Composition, Exempt).

Other devices from Shanghai May Skin Information Technology Co., Ltd.

See all devices from Shanghai May Skin Information Technology Co., Ltd. →

Properties

  • Premarket exempt
  • Serial number
  • Manufacturing date
Other properties (12, all answered No)