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Retractor, Spinal, quick-connect Blade blunt 24x35mm 29-3629.35

by Geister Medizin Technik GmbH

Ref 29-3629.35

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 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number4057034000000962X Basic UDI-DI 04057034101476UDI-DIDate9 Oct 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number04057034101476 UDI-DI Date18 Oct 2018ListedStatusListed 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  • Withdrawn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
Retractor, Spinal, quick-connect Blade blunt 24x35mm
Generic Name
Surgical retraction system mounting frame, reusable
Device Name
Retractor Blade Cone Mount Titanium Blunt
Model / Ref / Catalog
29-3629.35
Primary DI / UDI-DI
04057034101476
Basic UDI-DI
4057034000000962X
Direct Marketing DI
04057034101476
FDA Product Code
GZT
EMDN Code
L03140199 Spreaders and retractors for general surgery, reusable - other
GMDN Term
Surgical retraction system mounting frame, reusable
Device Class
Class IIa EUDAMED
Class II GUDID
Regulation Number
882.4800
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 II

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Properties

  • Prescription Use
  • Lot / Batch Number

Other properties (22)

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