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Rosch-Uchida G06929

by Cook Incorporated

Ref RUPS-100

Rosch-Uchida G06929 (RUPS-100) is a device classified as Class IIa in the EU and Class II in the US made by Cook Incorporated, registered in EUDAMED on 14 Sep 2026 (Basic UDI-DI B-00827002CINC31Y8) and listed in FDA GUDID since 6 May 2019 (UDI-DI D-00827002CINC31Y8), active as of 24 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 24 Oct 2026.

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD EUDAMED NumberB-00827002CINC31Y8 Basic UDI-DI D-00827002CINC31Y8UDI-DIDate14 Sep 2026RegisteredStatusActive
United StatesGUDID listing GUDID NumberD-00827002CINC31Y8 UDI-DI Date6 May 2019ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-00827002CINC31Y8 registered 14 Sep 2026 Active
  • FDA GUDID UDI-DI D-00827002CINC31Y8 listed 6 May 2019 Listed

Timeline

2 dated events

  1. Listed FDA GUDID D-00827002CINC31Y8
  2. Registered EUDAMED B-00827002CINC31Y8

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  • Withdrawn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
Rosch-Uchida
Generic name
Soft-tissue biopsy procedure kit, non-medicated
Device name
Rosch-UchidaTransjugular Liver Access Set
Model / Ref / Catalog
RUPS-100, G06929
Primary DI / UDI-DI
D-00827002CINC31Y8 EUDAMED
00827002069299 GUDID
Basic UDI-DI
B-00827002CINC31Y8
FDA product code
DYB
EMDN code
A01020199 Needles and kits for histological and cytological biopsy of soft tissues - other
GMDN term
Soft-tissue biopsy procedure kit, non-medicated
Device class
Class IIa EUDAMED
Class II GUDID
Regulation number
870.1340
EU registration type
Legacy device (under a directive)
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 3 fields differ

FieldEUDAMEDGUDID
Model / referenceEUDAMED
RUPS-100
GUDID
G06929
Primary DI / UDI-DIEUDAMED
D-00827002CINC31Y8
GUDID
00827002069299
Device classEUDAMED
Class IIa
GUDID
Class II

The registries describe this device under different primary UDI-DIs (EUDAMED lists D-00827002CINC31Y8; FDA GUDID lists 00827002069299), so their flags are not compared. Device class is stated on each registry's own scale: Class IIa 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: Soft-tissue biopsy procedure kit, non-medicated

Similar devices in this category

Other devices filed under NEEDLES AND KITS FOR HISTOLOGICAL AND CYTOLOGICAL BIOPSY OF SOFT TISSUES - OTHER.

Other devices from Cook Incorporated

See all devices from Cook Incorporated →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (17, all answered No)