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Springs

by Bernhard Förster GmbH 42 variants

Part of a family of 42 devices: see the family page

Ref -307-1012

Springs (-307-1012) is a device classified as Class IIa in the EU and Class I in the US made by Bernhard Förster GmbH, registered in EUDAMED on 17 Mar 2026 (Basic UDI-DI ++EFOR030101DM) and listed in FDA GUDID since 24 Sep 2019 (UDI-DI EFOR30710121), active as of 22 Oct 2026.

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

CE MDR

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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number++EFOR030101DM Basic UDI-DI EFOR30710121UDI-DIDate17 Mar 2026RegisteredStatusActive
United StatesGUDID listing GUDID NumberEFOR30710121 UDI-DI Date24 Sep 2019ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI ++EFOR030101DM registered 17 Mar 2026 Active
  • FDA GUDID UDI-DI EFOR30710121 listed 24 Sep 2019 Listed

Timeline

2 dated events

  1. Listed FDA GUDID EFOR30710121
  2. Registered EUDAMED ++EFOR030101DM

Coverage

2 jurisdictions

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  • Withdrawn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

Specification

EUDAMED · GUDID

Generic name
Orthodontic wire
Device name
Springs
Model / reference
-307-1012
Primary DI / UDI-DI
EFOR30710121
Basic UDI-DI
++EFOR030101DM
Unit of use DI
EFOR3071012001
FDA product code
DZC
EMDN code
Q010404 Orthodontic elastics, chains and springs
GMDN term
Orthodontic wire
Device class
Class IIa EUDAMED
Class I GUDID
Regulation number
872.5410
EU registration type
Standard device
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device classEUDAMED
Class IIa
GUDID
Class I

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

Manufacturer details

EUDAMED SRN
DE-MF-000006256

Similar devices in this category

Other devices filed under ORTHODONTIC ELASTICS, CHAINS AND SPRINGS.

Other devices from Bernhard Förster GmbH

See all devices from Bernhard Förster GmbH →

Properties

  • Single use
  • Contains CMR substances (carcinogenic, mutagenic or toxic to reproduction)
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (19, all answered No)