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Ibramed Dermotonus Esthetic

by Ibramed Industria Brasileira de Equipamentos Medicos Eir 2 variants

Ibramed Dermotonus Esthetic (01006005) is a Class I device made by Ibramed Industria Brasileira de Equipamentos Medicos Eir, listed in FDA GUDID since 13 Oct 2017 (UDI-DI 07898961579139), 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 Number07898961579139 UDI-DI Date13 Oct 2017ListedStatusListed 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  • Withdrawn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
Ibramed
Generic name
Dermabrasion unit
Model / Ref / Catalog
Dermotonus Esthetic, 01006005
Primary DI / UDI-DI
07898961579139
FDA product code
GFE
GMDN term
Dermabrasion unit
Device class
Class I
Regulation number
878.4820
GUDID distribution status
In Commercial Distribution

Related devices

Category: Skin abrasion unit

Similar devices

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

Other devices from Ibramed Industria Brasileira de Equipamentos Medicos Eir

See all devices from Ibramed Industria Brasileira de Equipamentos Medicos Eir →

Properties

  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Serial number
  • Manufacturing date
Other properties (10, all answered No)