Skip to content

DIPLOMAT Faszia cutter, cannulated

by SIGNUS Medizintechnik GmbH

Ref AC0150Model Cutter

DIPLOMAT Faszia cutter, cannulated (AC0150) is a Class I device made by SIGNUS Medizintechnik GmbH, registered in EUDAMED on 28 Oct 2026 (Basic UDI-DI 4047844020597440211DA) and listed in FDA GUDID since 21 May 2025 (UDI-DI 04047844044490), active as of 7 Nov 2026.

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

CE MDR

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 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number4047844020597440211DA Basic UDI-DI 04047844044490UDI-DIDate28 Oct 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number04047844044490 UDI-DI Date21 May 2025ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 4047844020597440211DA registered 28 Oct 2026 Active
  • FDA GUDID UDI-DI 04047844044490 listed 21 May 2025 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 04047844044490
  2. Registered EUDAMED 4047844020597440211DA

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  • Withdrawn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
Diplomat Mis EUDAMED
Diplomat GUDID
Generic name
Orthopaedic surgical procedure kit, non-medicated, reusable
Model / Ref / Catalog
Cutter, AC0150, Faszia cutter, cannulated
Primary DI / UDI-DI
04047844044490
Basic UDI-DI
4047844020597440211DA
Direct marketing DI
04047844044490
FDA product code
LXH
EMDN code
L0103 Dermotomes and blades, reusable
GMDN term
Orthopaedic surgical procedure kit, non-medicated, reusable
Device class
Class I
Regulation number
888.4540
System or procedure pack
System which is a device in itself
EU registration type
Standard device
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Model / referenceEUDAMED
Cutter
AC0150
GUDID
Faszia cutter, cannulated

Similar devices in this category

Other devices filed under DERMOTOMES AND BLADES, REUSABLE.

Other devices from SIGNUS Medizintechnik GmbH

See all devices from SIGNUS Medizintechnik GmbH →

Properties

  • Sterilise before use
  • Reusable
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (19, all answered No)