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Navigation Enabled Instruments

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref 3010-19-025Model Navigation Enabled Instruments for the Thoracic-Lumbar-Sacral Spine

by Medos International SARL

Identity

Trade Name
NAVIGATION ENABLED INSTRUMENTS EUDAMED
NA FDA UDI
Generic Name
Bone tap, reusable FDA UDI
Device Name
Navigation Enabled Driver Shaft Sleeve Awl Tip Tap for the Thoracic-Lumbar-Sacral Spine EUDAMED
NAVIGATION ENABLED INSTRUMENTS DUAL LEAD AWL TIP TAP 8MM FDA UDI
Model / Reference
Navigation Enabled Instruments for the Thoracic-Lumbar-Sacral Spine EUDAMED
3010-19-025 EUDAMEDFDA UDI
Description
NAVIGATION ENABLED INSTRUMENTS DUAL LEAD AWL TIP TAP 8MM FDA UDI

Identifiers

Catalog Number
301019025 FDA UDI
Primary DI / UDI-DI
10705034561516 EUDAMEDFDA UDI
Basic UDI-DI
0705034a002355Z EUDAMED
Direct Marketing DI
10705034561516 EUDAMED
FDA Product Code
OLO FDA UDI
EMDN Code
Z12130480 STEREOTACTIC ORTHOPAEDIC SURGERY INSTRUMENTS - HARDWARE ACCESSORIES EUDAMED
GMDN Term
Bone tap, reusable FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class II FDA UDI
Regulation Number
882.4560 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

No

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

No

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: Multi-purpose stereotactic surgery system

Navigation Enabled Instruments by Medos International Sarl — Class IIa — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Multi-purpose stereotactic surgery system.

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 bcaf3a86-bbbe-45a6-aa76-721792ad7db8 61 fields · synced May 30, 2026
  • FDA UDI 6f3649a6-8037-4b9f-b34a-1fe203ae049e 35 fields · synced May 30, 2026