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MM MARKED PAPER POINTS DIA-PRO W Primary

by DiaDent Group International

Ref MP265-602Model MM MARKED PAPER POINTS DIA-PRO W #Primary

MM MARKED PAPER POINTS DIA-PRO W Primary (MP265-602) is a device classified as Class IIa in the EU and Class I in the US made by DiaDent Group International, registered in EUDAMED on 30 Oct 2026 (Basic UDI-DI B-08806383543545) and listed in FDA GUDID since 25 May 2020 (UDI-DI 08806383543545), active as of 7 Nov 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 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD EUDAMED NumberB-08806383543545 Basic UDI-DI 08806383543545UDI-DIDate30 Oct 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number08806383543545 UDI-DI Date25 May 2020ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-08806383543545 registered 30 Oct 2026 Active
  • FDA GUDID UDI-DI 08806383543545 listed 25 May 2020 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 08806383543545
  2. Registered EUDAMED B-08806383543545

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  • Withdrawn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
Absorbent Paper Points EUDAMED
Mm Marked Paper Points GUDID
Generic name
Endodontic paper point
Model / Ref / Catalog
MM MARKED PAPER POINTS DIA-PRO W #Primary, MP265-602, DIA-PRO W Primary
Primary DI / UDI-DI
08806383543545
Basic UDI-DI
B-08806383543545
FDA product code
EKN
EMDN code
Q01010401 Paper and gutta-percha tips, matrices and wedges for dentistry
GMDN term
Endodontic paper point
Device class
Class IIa EUDAMED
Class I GUDID
Regulation number
872.3830
EU registration type
Legacy device (under a directive)
EU market of registration
Netherlands
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 2 fields differ

FieldEUDAMEDGUDID
Model / referenceEUDAMED
MM MARKED PAPER POINTS DIA-PRO W #Primary
MP265-602
GUDID
DIA-PRO W Primary
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.

Related devices

Category: Endodontic paper point

Similar devices in this category

Other devices filed under PAPER AND GUTTA-PERCHA TIPS, MATRICES AND WEDGES FOR DENTISTRY.

Other devices from DiaDent Group International

See all devices from DiaDent Group International →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Premarket exempt
Other properties (19, all answered No)