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Ezx BRELL039

by Imedicom Co., Ltd.

Ezx BRELL039 is a Class I device made by Imedicom Co., Ltd., listed in FDA GUDID since 7 Feb 2020 (UDI-DI 08800038038950), 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 Number08800038038950 UDI-DI Date7 Feb 2020ListedStatusListed 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  • Withdrawn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
Ezx
Generic name
Sawing power tool attachment, sagittal
Model / reference
BRELL039
Primary DI / UDI-DI
08800038038950
FDA product code
HWE
GMDN term
Sawing power tool attachment, sagittal
Device class
Class I
Regulation number
878.4820
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Sawing power tool attachment, sagittal

Similar devices in this category

Other devices filed under Sawing power tool attachment, sagittal.

Other devices from Imedicom Co., Ltd.

See all devices from Imedicom Co., Ltd. →

Properties

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