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Origins 830-Hdaslulk

by Solta Medical, Inc.

Ref 830-HDASLULK

Origins 830-Hdaslulk is a device classified as Class IIa in the EU and Class II in the US made by Solta Medical, Inc., registered in EUDAMED on 15 Jun 2026 (Basic UDI-DI B-00850608002735) and listed in FDA GUDID since 23 Sep 2016 (UDI-DI 00850608002735), active as of 24 Oct 2026.

Active European Union. Also listed in GUDID (US).

CE MDD

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, GUDID, synced 24 Oct 2026.

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD EUDAMED NumberB-00850608002735 Basic UDI-DI 00850608002735UDI-DIDate15 Jun 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00850608002735 UDI-DI Date23 Sep 2016ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-00850608002735 registered 15 Jun 2026 Active
  • FDA GUDID UDI-DI 00850608002735 listed 23 Sep 2016 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 00850608002735
  2. Registered EUDAMED B-00850608002735

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDD Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Trade name
Origins
Generic name
Liposuction system
Device name
Origins Handle, Aspiration, LL
Model / Ref / Catalog
830-HDASLULK
Primary DI / UDI-DI
00850608002735
Basic UDI-DI
B-00850608002735
FDA product code
MUU
EMDN code
L250399 Liposuction instruments, reusable - other
GMDN term
Liposuction system
Device class
Class IIa EUDAMED
Class II GUDID
Regulation number
878.5040
EU registration type
Legacy device (under a directive)
EU market of registration
Netherlands
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device classEUDAMED
Class IIa
GUDID
Class II

Device class is stated on each registry's own scale: Class IIa in the EU (EUDAMED), Class II in the US (FDA GUDID). EU and US classes are different schemes, so this is not a disagreement.

Related devices

Category: Liposuction system

Similar devices in this category

Other devices filed under LIPOSUCTION INSTRUMENTS, REUSABLE - OTHER.

Other devices from Solta Medical, Inc.

See all devices from Solta Medical, Inc. →

Properties

  • Sterilise before use
  • Prescription use
  • Lot / batch number
  • Manufacturing date
Other properties (19, all answered No)