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Curette Flexible 10mm-w/Dual Port Design

by Medgyn International, Inc

Ref 022010

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

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/MDD EUDAMED NumberB-M803022010 Basic UDI-DI M803022010UDI-DIDate17 Oct 2023RegisteredStatusActive
United StatesGUDID listing GUDID NumberM803022010 UDI-DI Date7 Sep 2016ListedStatusListed 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  • Withdrawn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/MDD Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Trade Name
MedGyn Uterine Curette
Generic Name
Intrauterine cannula, single-use
Device Name
Curette Flexible 10mm-w/Dual Port Design
Model / Ref / Catalog
022010, 10mm flexible curette
Primary DI / UDI-DI
M803022010
Basic UDI-DI
B-M803022010
FDA Product Code
HCY
EMDN Code
U089010 Uterine curettes, single-use
GMDN Term
Intrauterine cannula, single-use
Device Class
Class I
Regulation Number
884.4530
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution
MRI Safety
MR Safe

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Model / ReferenceEUDAMED
022010
GUDID
10mm flexible curette

Manufacturer details

EUDAMED SRN
US-MF-000031450
Authorised representative
Advena Limited MT-AR-000000234

Other devices from Medgyn International, Inc

See all devices from Medgyn International, Inc →

Properties

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

Other properties (16)

  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: 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