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Expedium Spine System

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 279702500Model Measuring Instruments -Taps

by Medos International SARL

Identity

Trade Name
EXPEDIUM SPINE SYSTEM EUDAMED
EXPEDIUM FDA UDI
Generic Name
Bone tap, reusable FDA UDI
Device Name
Reusable Bone Taps EUDAMED
EXPEDIUM SPINE SYSTEM DOUBLE-LEAD TAP 5.0mm 30-50mm Plus or Minus 1.33 Percent FDA UDI
Model / Reference
Measuring Instruments -Taps EUDAMED
279702500 EUDAMEDFDA UDI
Description
EXPEDIUM SPINE SYSTEM DOUBLE-LEAD TAP 5.0mm 30-50mm Plus or Minus 1.33 Percent FDA UDI

Identifiers

Catalog Number
279702500 FDA UDI
Primary DI / UDI-DI
10705034198613 EUDAMEDFDA UDI
Basic UDI-DI
0705034a001876F EUDAMED
Direct Marketing DI
10705034198613 EUDAMED
FDA Product Code
HWX FDA UDI
EMDN Code
L091099 OSTEOSYNTHESIS INSTRUMENTS, REUSABLE - OTHER EUDAMED
GMDN Term
Bone tap, reusable FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
888.4540 FDA UDI
Market of Registration
Belgium EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

Yes

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

Yes

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

Yes

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Surgical implant template, reusable

Expedium Spine System by Medos International Sarl — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical implant template, reusable.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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Manufacturer

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

Sources (2)

  • EUDAMED 14e4f8f6-9339-45c4-9c51-dc42d961c311 61 fields · synced Jun 8, 2026
  • FDA UDI d6f036af-fcbf-4edc-8408-a77f5a93cb93 35 fields · synced May 29, 2026