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Expedium Anterior Spine System

by Medos International SARL 52 variants

Ref 187702530, 187702760, 187702747, 187702727, 187702620, 187702725, 187702730, 187702522, 187703100, 187704014, 287710105, 187702622, 187702637, 187702520, 187702745, 287720160, 287710700Model ‌EXPEDIUM ANTERIOR SPINE SYSTEM - SCREWS, ‌EXPEDIUM ANTERIOR SPINE SYSTEM - RODS, ‌EXPEDIUM ANTERIOR SPINE SYSTEM - CROSS CONNECTORS, Expedium Anterior Osteosynthesis Instruments, Expedium Anterior Instruments for Insertion and Extraction of Osteosynthesis Devices, Measuring Instruments -Taps

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 24 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 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number0705034a001805Z Basic UDI-DI Date14 Oct 2025RegisteredStatusActive
United StatesGUDID listing GUDID Number10705034138381 UDI-DI Date24 Sep 2015ListedStatusListed 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 24 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  • Withdrawn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
Expedium Anterior Spine System EUDAMED
Expedium GUDID
Generic Name
Bone-screw internal spinal fixation system connector
Orthopaedic fixation implant alignment tool
Spinal bone screw, non-bioabsorbable
Bone tap, reusable
Surgical implant template, reusable
Bone-screw internal spinal fixation system rod
Device Name
‌screws for Thoracolumbosacral Spine Fixation
‌rods for Thoracolumbosacral Spine Fixation
Cross Connectors for Thoracolumbosacral Spine Fixation
Expedium Anterior Instruments Template Stabilizer
Expedium Anterior Instruments Guide Holder Impactor Distractor Driver Shaft Wrench
Reusable Bone Taps
Model / Ref / Catalog
‌EXPEDIUM ANTERIOR SPINE SYSTEM - SCREWS, 187702530, 187702760, 187702747, 187702727, 187702620, 187702725, 187702730, 187702522, 187704014, 287720160, 187702637, 187702745, 287710700, 287710105, 187703100, ‌EXPEDIUM ANTERIOR SPINE SYSTEM - RODS, ‌EXPEDIUM ANTERIOR SPINE SYSTEM - CROSS CONNECTORS, Expedium Anterior Osteosynthesis Instruments, 187702622, 187702520, Expedium Anterior Instruments for Insertion and Extraction of Osteosynthesis Devices, Measuring Instruments -Taps
Primary DI / UDI-DI
10705034138381, 10705034138848, 10705034138794, 10705034138718, 10705034138510, 10705034138701, 10705034138725, 10705034138350, 10705034139081, 10705034219509, 10705034138589, 10705034138787, 10705034219417, 10705034219264, 10705034138961, 10705034138527, 10705034138343
Basic UDI-DI
0705034a001805Z, 0705034a001796G, 0705034a001786E, 0705034a001215H, 0705034a001205F, 0705034a001876F
Direct Marketing DI
10705034219264
10705034219509
10705034219417
510(k) Number
FDA Product Code
KWQ, LXH, HWX, HWT
EMDN Code
P09070302, L091099, L091001
GMDN Term
Bone-screw internal spinal fixation system connector
Orthopaedic fixation implant alignment tool
Spinal bone screw, non-bioabsorbable
Bone tap, reusable
Surgical implant template, reusable
Bone-screw internal spinal fixation system rod
Device Class
Class IIb EUDAMED
Class I EUDAMEDGUDID
Class II GUDID
Regulation Number
888.3060, 888.4540, 888.4800
EU 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 IIb
Class I
GUDID
Class I
Class II

Manufacturer details

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

Related devices

Category: Spinal bone screw, non-bioabsorbable

Other devices from Medos International SARL

See all devices from Medos International SARL →

Properties

  • Single Use YesGUDIDNoGUDID
  • Implantable YesEUDAMEDGUDIDNoEUDAMEDGUDID
  • Reusable NoEUDAMEDYesEUDAMED
  • Sutures
  • CMR Substance NoEUDAMEDYesEUDAMED
  • Measuring Function NoEUDAMEDYesEUDAMED
  • Prescription Use
  • Premarket Exempt NoGUDIDYesGUDID
  • Lot / Batch Number

Other properties (16)

  • Sterile: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: 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