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Laparoscopic Retractors

by Mediflex Surgical Product

Ref 69703

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number08421021LR5E Basic UDI-DI 00842102107535UDI-DIDate6 Jan 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00842102107535 UDI-DI Date11 Jan 2019ListedStatusListed 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  • Withdrawn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
Laparoscopic Retractors EUDAMED
Holders and Positioners - Nathanson Hooks GUDID
Generic Name
Surgical retraction system, reusable
Model / Reference
69703
Primary DI / UDI-DI
00842102107535
Basic UDI-DI
08421021LR5E
Direct Marketing DI
00842102107535
FDA Product Code
FFO
EMDN Code
L1206 Laparoscopic and thoracoscopic surgery spreaders and retractors, reusable
GMDN Term
Surgical retraction system, reusable
Device Class
Class I
Regulation Number
876.4730
EU market of registration
Spain
GUDID distribution status
In Commercial Distribution
Sterilization Method
Moist Heat or Steam Sterilization

Manufacturer details

EUDAMED SRN
US-MF-000026992
Authorised representative
Emergo Europe B.V. NL-AR-000000116

Other devices from Mediflex Surgical Product

Properties

  • Reusable
  • Premarket Exempt
  • Manufacturing Date

Other properties (21)

  • Sterile: No
  • Single Use: No
  • Implantable: 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
  • Prescription Use: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Lot / Batch Number: No
  • Serial Number: No
  • Expiration Date: No