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Dornier MedTech Medilas D30 1064 (SMA)

by Dornier MedTech GmbH

Dornier MedTech Medilas D30 1064 (SMA) (K2012015) is a Class II device made by Dornier MedTech GmbH, listed in FDA GUDID since 12 Sep 2018 (UDI-DI 04049958002090), 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 Number04049958002090 UDI-DI Date12 Sep 2018ListedStatusListed 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  • Withdrawn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
Dornier MedTech
Generic name
General/multiple surgical diode laser system
Model / Ref / Catalog
Medilas D30 1064 (SMA), K2012015
Primary DI / UDI-DI
04049958002090
FDA product code
GEX
GMDN term
General/multiple surgical diode laser system
Device class
Class II
Regulation number
878.4810
GUDID distribution status
In Commercial Distribution

Related devices

Category: General/multiple surgical diode laser system

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Other devices filed under General/multiple surgical diode laser system.

Other devices from Dornier MedTech GmbH

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Properties

  • Serial number
  • Manufacturing date
Other properties (13, all answered No)