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Contra Elite Extend Flex DPA

by Young Dental Manufacturing I, LLC

Ref 157020, 157012Model Disposable Prophy Angle

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

CE MDR CE MDD

Valid until

Not listed

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

Registry data, not yet checked by deviCERTS. Source EUDAMED, GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED NumberB-10302731570201 Basic UDI-DI Date21 Nov 2022RegisteredStatusActive
European UnionCE/MDD EUDAMED NumberB-10302731570201 Basic UDI-DI Date21 Nov 2022RegisteredStatusActive
United StatesGUDID listing GUDID Number10302731570201 UDI-DI Date16 Oct 2022ListedStatusListed GUDID: in commercial distribution

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

2 jurisdictions

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  • Withdrawn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

Specification

EUDAMED · GUDID

Trade Name
Contra Elite Extend Flex DPA EUDAMED
Young GUDID
Generic Name
Dental polishing cup, single-use
Model / Ref / Catalog
157020, 157012, Disposable Prophy Angle
Primary DI / UDI-DI
10302731570201 EUDAMED
10302731570126 EUDAMED
00302731570129 GUDID
00302731570204 GUDID
Basic UDI-DI
B-10302731570201, B-10302731570126, 03027346938K780752EGSK4
FDA Product Code
EGS
EMDN Code
Q01010403 Dental abrasive and polishing materials
GMDN Term
Dental polishing cup, single-use
Device Class
Class IIa EUDAMED
Class I GUDID
Regulation Number
872.4200
EU market of registration
Ireland
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 2 fields differ

FieldEUDAMEDGUDID
Primary DI / UDI-DIEUDAMED
10302731570201
10302731570126
GUDID
00302731570129
00302731570204
Device ClassEUDAMED
Class IIa
GUDID
Class I

Manufacturer details

EUDAMED SRN
US-MF-000027132
Authorised representative
Young Microbrush Ireland Ltd IE-AR-000011249

Other devices from Young Dental Manufacturing I, LLC

See all devices from Young Dental Manufacturing I, LLC →

Properties

  • Single Use
  • Prescription Use
  • Lot / Batch Number
  • Expiration Date
  • Manufacturing Date

Other properties (19)

  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No