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Dissector, Dura, acc. Penfield Fig. 4 20.5cm 28-0044

by Geister Medizin Technik GmbH

Ref 28-0044

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

CE MDR

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 24 Oct 2026. What this means

Overview

Dissector, Dura, acc. Penfield Fig. 4 20.5cm is a high-grade stainless steel manual surgical instrument designed for cutting and excising bone tissue in orthopaedic or plastic surgery procedures. It features a long, slender handle with a concave, spoon-like tip and sharp edge at the distal end.

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number40570340000000522MW Basic UDI-DI 04057034087404UDI-DIDate8 Oct 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number04057034087404 UDI-DI Date12 Sep 2023ListedStatusListed 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  • Withdrawn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 Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Trade Name
Dissector, Dura, acc. Penfield Fig. 4 20.5cm
Generic Name
Bone curette, reusable
Device Name
Kürette
Model / Ref / Catalog
28-0044
Primary DI / UDI-DI
04057034087404
Basic UDI-DI
40570340000000522MW
Direct Marketing DI
04057034087404
FDA Product Code
HTR
EMDN Code
L0315 General surgery dissectors, reusable
GMDN Term
Bone curette, reusable
Device Class
Class I
Regulation Number
878.4800
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution

Related devices

Category: Bone curette, reusable

Other devices from Geister Medizin Technik GmbH

See all devices from Geister Medizin Technik GmbH →

Properties

  • Reusable
  • Prescription Use
  • Premarket Exempt
  • Lot / Batch Number

Other properties (20)

  • Sterile: No
  • Single Use: No
  • Implantable: 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
  • Serial Number: No
  • Expiration Date: No
  • Manufacturing Date: No