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CONDUIT Lateral

by Medos International SARL 36 variants

Ref LET80859T, LEC00102C, LET01661T, LET81260T, LET01259T, LEC00101CModel Conduit Lumbar Trials, Conduit Cases and Trays for Spinal Medical Devices

Active European Union. Also listed in GUDID (US).

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

None found

in data synced 22 Oct 2026

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 Number0705034a002005E Basic UDI-DI Date18 Nov 2025RegisteredStatusActive
United StatesGUDID listing GUDID Number10705034556673 UDI-DI Date24 Sep 2021ListedStatusListed 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.

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 22 Oct 2026.

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  • Withdrawn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
CONDUIT Lateral EUDAMED
Conduit GUDID
Generic Name
Surgical instrument/implant rack
Spinal implant trial
Device Name
Conduit Trial
Conduit Cases and Trays for Spinal Medical Devices
Model / Ref / Catalog
Conduit Lumbar Trials, LET80859T, LEC00102C, LEC00101C, LET01661T, LET01259T, LET81260T, Conduit Cases and Trays for Spinal Medical Devices
Primary DI / UDI-DI
10705034556673, 10705034556192, 10705034556185, 10705034556987, 10705034556260, 10705034556901
Basic UDI-DI
0705034a002005E, 0705034a000415J
Direct Marketing DI
10705034556673
10705034556192
10705034556987
10705034556901
10705034556260
10705034556185
510(k) Number
FDA Product Code
FSM, MAX
EMDN Code
L091001, V0499
GMDN Term
Surgical instrument/implant rack
Spinal implant trial
Device Class
Class IIa EUDAMED
Class I EUDAMEDGUDID
Class II GUDID
Regulation Number
878.4800, 888.3080
Market of Registration
Belgium
GUDID distribution status
In Commercial Distribution
Sterilization Method
Moist Heat or Steam Sterilization

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device ClassEUDAMED
Class IIa
Class I
GUDID
Class I
Class II

Manufacturer details

EUDAMED SRN
CH-MF-000014268
Authorised representative
DePuy Ireland UC IE-AR-000009328

Other devices from Medos International SARL

See all devices from Medos International SARL →

Properties

  • Reusable YesEUDAMEDNoEUDAMED
  • CMR Substance YesEUDAMEDNoEUDAMED
  • Prescription Use
  • Premarket Exempt YesGUDIDNoGUDID
  • Lot / Batch Number

Other properties (19)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Reprocessed: 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
  • Serial Number: No
  • Expiration Date: No
  • Manufacturing Date: No