Pricing Sign in

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Partners Contact

Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

Mountaineer Clamp Tap Drill Bender… — 17 UDI-DI variants, MDR

MD Atlas
Medos International SARL

Data from EUDAMED, last updated May 23, 2026

Mountaineer Clamp Tap Drill Bender Feeler Torque Template

0705034a001465Z

17 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class I

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: Medos International SARL

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

Device characteristics

Reusable

Identity & classification

Basic UDI-DI: 0705034a001465Z
Device name: Mountaineer Clamp Tap Drill Bender Feeler Torque Template
Device model: MOUNTAINEER OSTEOSYNTHESIS INSTRUMENTS, REUSABLE - OTHER
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Dec 30, 2025

Manufacturer & authorised representative

Manufacturer

Name: Medos International SARL
SRN: CH-MF-000014268
Country: Switzerland
Email: EUDAMED_Enquiries@its.jnj.com
Phone: +41 32 934 80 00

Authorised representative

Name: DePuy Ireland UC
SRN: IE-AR-000009328
Country: Ireland
Phone: +353 (0)21 4914000

Variants by status

UDI-DI variants

17 UDI-DI variants

Sign in to export

Exports are reserved for signed-in users. Sign in or create an account to continue.

Email

Password

No account yet?

Export results

Applied filters

basicUdiUlid01KDR9RBF1N3K46T31S6JAZDD9

Format

Summary

29 columns included

Trade name
Basic UDI-DI
UDI-DI code
Risk category
Applicable legislation
Status
Organization name
SRN
Reference / catalog number
Additional product description
Intended medical purpose
Placed on the market (country)
Market info update date
Sterile
Single use
Contains latex
Reprocessed single-use
Direct marking
CMR substance
Endocrine disruptor
Annex XVI applicable
Sterilization
OEM applicable
EMDN codes
Last updated
Basic UDI-DI device name
Basic UDI-DI device model
Basic UDI-DI implantable
Basic UDI-DI reagent

MOUNTAINEER OCT SPINAL SYSTEM10705034221526
MOUNTAINEER OCT SPINAL SYSTEM10705034221854
MOUNTAINEER OCT SPINAL SYSTEM10705034221502
MOUNTAINEER OCT SPINAL SYSTEM10705034221465
MOUNTAINEER OCT SPINAL SYSTEM10705034221823
MOUNTAINEER OCT SPINAL SYSTEM10705034221748
MOUNTAINEER OCT SPINAL SYSTEM10705034221687
MOUNTAINEER OCT SPINAL SYSTEM10705034221410
MOUNTAINEER OCT SPINAL SYSTEM10705034221755
MOUNTAINEER OCT SPINAL SYSTEM10705034221670
MOUNTAINEER OCT SPINAL SYSTEM10705034221380
SUMMIT OCT SPINAL FIXATION SYSTEM10705034193434
SUMMIT SI OCT SPINAL FIXATION SYSTEM10705034193090
SUMMIT SI OCT SPINAL FIXATION SYSTEM10705034193403
SUMMIT SI OCT SPINAL FIXATION SYSTEM10705034193359
SUMMIT SI OCT SPINAL FIXATION SYSTEM10705034193380
SUMMIT SI OCT SPINAL FIXATION SYSTEM10705034193397