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Pipelle®

by Laboratoire Ccd

Ref 1103000Model 2023B1

Pipelle (1103000) is a cervical cytology brush (EU MDD Class I; FDA Class II; FDA product code HHK, Curette, Suction, Endometrial (and Accessories)) made by Laboratoire Ccd, registered in EUDAMED on 22 Sep 2026 (Basic UDI-DI B-03700111400719) and listed in FDA GUDID since 5 Dec 2023 (UDI-DI 03700111400719), active as of 7 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 7 Oct 2026.

Regulatory status

as of registry sync 7 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD EUDAMED NumberB-03700111400719 Basic UDI-DI 03700111400719UDI-DIDate22 Sep 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number03700111400719 UDI-DI Date5 Dec 2023ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-03700111400719 registered 22 Sep 2026 Active
  • FDA GUDID UDI-DI 03700111400719 listed 5 Dec 2023 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 03700111400719
  2. Registered EUDAMED B-03700111400719

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  • Withdrawn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

Generic name
Cervical cytology brush
Model / Ref / Catalog
2023B1, 1103000, PIPELLE®
Primary DI / UDI-DI
03700111400719
Basic UDI-DI
B-03700111400719
FDA product code
HHK
EMDN code
U089002 Devices for gynaecological cytology
GMDN term
Cervical cytology brush
Device class
Class I EUDAMED
Class II GUDID
Regulation number
884.1175
EU registration type
Legacy device (under a directive)
EU market of registration
France
GUDID distribution status
In Commercial Distribution
Size
Catheter Length — 23.5 Centimeter
Outer Diameter — 0.31 Centimeter

Truth per registry

2 sources · 2 fields differ

FieldEUDAMEDGUDID
Model / referenceEUDAMED
2023B1
1103000
GUDID
PIPELLE®
Device classEUDAMED
Class I
GUDID
Class II

Device class is stated on each registry's own scale: Class I 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: Cervical cytology brush

Similar devices in this category

Other devices filed under DEVICES FOR GYNAECOLOGICAL CYTOLOGY.

Other devices from Laboratoire Ccd

See all devices from Laboratoire Ccd →

Properties

  • Supplied sterile
  • Single use
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (20, all answered No)