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Superpath® 20071006

by MicroPort Orthopedics Inc.

Ref 20071006

Superpath® 20071006 is a Class I device made by MicroPort Orthopedics Inc., registered in EUDAMED on 3 Nov 2026 (Basic UDI-DI 0192629IRHL0901QZ) and listed in FDA GUDID since 16 Feb 2017 (UDI-DI 00192629113237), 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 Number0192629IRHL0901QZ Basic UDI-DI 00192629113237UDI-DIDate3 Nov 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00192629113237 UDI-DI Date16 Feb 2017ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 0192629IRHL0901QZ registered 3 Nov 2026 Active
  • FDA GUDID UDI-DI 00192629113237 listed 16 Feb 2017 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 00192629113237
  2. Registered EUDAMED 0192629IRHL0901QZ

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  • Withdrawn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
Superpath® Calcar Curette EUDAMED
Superpath® GUDID
Generic name
Joint prosthesis implantation kit, reusable
Device name
Hip Orthopaedic surgery spoons and curettes, reusable
Model / Ref / Catalog
20071006
Primary DI / UDI-DI
00192629113237 EUDAMED
M684200710061 GUDID
Basic UDI-DI
0192629IRHL0901QZ
Secondary DI
M684200710061
Direct marketing DI
00192629113237
FDA product code
HTF
EMDN code
L0901 Orthopaedic surgery spoons and curettes, reusable
GMDN term
Joint prosthesis implantation kit, reusable
Device class
Class I
Regulation number
878.4800
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
Primary DI / UDI-DIEUDAMED
00192629113237
GUDID
M684200710061

The registries describe this device under different primary UDI-DIs (EUDAMED lists 00192629113237; FDA GUDID lists M684200710061), so their flags are not compared.

Related devices

Category: Joint prosthesis implantation kit, reusable

Similar devices in this category

Other devices filed under ORTHOPAEDIC SURGERY SPOONS AND CURETTES, REUSABLE.

Other devices from MicroPort Orthopedics Inc.

See all devices from MicroPort Orthopedics Inc. →

Properties

  • Sterilise before use
  • Reusable
  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (20, all answered No)