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Retractor, Spinal, blade blunt, channeli 45mm narrow 29-3033.45

by Geister Medizin Technik GmbH

Ref 29-3033.45

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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number40570340000008932 Basic UDI-DI 04057034097892UDI-DIDate9 Oct 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number04057034097892 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  • Withdrawn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, blade blunt, channeli 45mm narrow
Generic Name
Surgical retraction system mounting frame, reusable
Device Name
Retractor Blade Round Head Mount PEEK Blunt
Model / Ref / Catalog
29-3033.45
Primary DI / UDI-DI
04057034097892
Basic UDI-DI
40570340000008932
Direct Marketing DI
04057034097892
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