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Superpath® 2007XL07

by MicroPort Orthopedics Inc.

Ref 2007XL07

Superpath® 2007XL07 is a device classified as Class IIa in the EU and Class I in the US made by MicroPort Orthopedics Inc., registered in EUDAMED on 3 Nov 2026 (Basic UDI-DI 0192629IIAHP091303HT) and listed in FDA GUDID since 8 Apr 2021 (UDI-DI 00192629260818), 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 Number0192629IIAHP091303HT Basic UDI-DI 00192629260818UDI-DIDate3 Nov 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00192629260818 UDI-DI Date8 Apr 2021ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 0192629IIAHP091303HT registered 3 Nov 2026 Active
  • FDA GUDID UDI-DI 00192629260818 listed 8 Apr 2021 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 00192629260818
  2. Registered EUDAMED 0192629IIAHP091303HT

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  • Withdrawn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® Screw Drill Bit X-Long, Sterile EUDAMED
Superpath® GUDID
Generic name
Surgical instrument/implant depth limiter, reusable
Device name
Hip Orthopaedic Implant Drill Bits, Single-Use
Model / Ref / Catalog
2007XL07
Primary DI / UDI-DI
00192629260818
Basic UDI-DI
0192629IIAHP091303HT
Secondary DI
M6842007XL071
Direct marketing DI
00192629260818
FDA product code
HTW
EMDN code
P091303 Orthopaedic implant drill bits, single-use
GMDN term
Surgical instrument/implant depth limiter, reusable
Device class
Class IIa EUDAMED
Class I GUDID
Regulation number
888.4540
EU registration type
Standard device
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device classEUDAMED
Class IIa
GUDID
Class I

Device class is stated on each registry's own scale: Class IIa in the EU (EUDAMED), Class I in the US (FDA GUDID). EU and US classes are different schemes, so this is not a disagreement.

Related devices

Category: Surgical instrument/implant depth limiter, reusable

Similar devices in this category

Other devices filed under ORTHOPAEDIC IMPLANT DRILL BITS, SINGLE-USE.

Other devices from MicroPort Orthopedics Inc.

See all devices from MicroPort Orthopedics Inc. →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (18, all answered No)