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Cosmopen Tips -Type A

by CosmoFrance

Cosmopen Tips -Type A (CPMNT030) is a Class I device made by CosmoFrance, listed in FDA GUDID since 2 Apr 2024 (UDI-DI G589CPMNT030), 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 NumberG589CPMNT030 UDI-DI Date2 Apr 2024ListedStatusListed GUDID: 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  • Withdrawn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
Cosmopen
Generic name
Dermabrasion brush, rotary
Model / Ref / Catalog
Cosmopen Tips -Type A, CPMNT030
Primary DI / UDI-DI
G589CPMNT030
FDA product code
GFE
GMDN term
Dermabrasion brush, rotary
Device class
Class I
Regulation number
878.4820
GUDID distribution status
In Commercial Distribution
Sterilisation method
Radiation Sterilization

Related devices

Category: Dermabrasion brush, rotary

Similar devices

Other devices filed under FDA product code GFE (Brush, Dermabrasion, Powered).

Other devices from CosmoFrance

See all devices from CosmoFrance →

Properties

  • Supplied sterile
  • Sterilise before use
  • Single use
  • Convenience kit
  • Combination product
  • Lot / batch number
  • Expiration date
Other properties (8, all answered No)