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Perfectio 900

by zhongshan Bisen plastic electronic products CO, LTD

Listed FDA GUDID listing, not in commercial distribution

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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number16928336800389 UDI-DI Date11 Oct 2016ListedStatusListed GUDID: not in commercial distribution

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Perfectio
Generic Name
Cosmetic red-light phototherapy system, home-use
Model / Reference
900
Primary DI / UDI-DI
16928336800389
FDA Product Code
OHS
GMDN Term
Cosmetic red-light phototherapy system, home-use
Device Class
Class II
Regulation Number
878.4810
GUDID distribution status
Not in Commercial Distribution
MRI Safety
MR Conditional

Other devices from zhongshan Bisen plastic electronic products CO, LTD

Properties

  • Over-the-Counter
  • Lot / Batch Number
  • Manufacturing Date

Other properties (11)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Expiration Date: No