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.

Polyaxial, Uniplanar Screws — 64 UDI-DI variants, MDR

MD Atlas
Medos International SARL

Data from EUDAMED, last updated May 23, 2026

Polyaxial, Uniplanar Screws

0705034a002576B

64 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
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

Implantable

Identity & classification

Basic UDI-DI: 0705034a002576B
Device name: Polyaxial, Uniplanar Screws
Device model: TriALTIS Spine System Bone Screw Fenestrated
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
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

64 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

basicUdiUlid01KDRG899KV4HENHRKQ4PQ2XC5

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

TRIALTIS Spine System10705034585246
TRIALTIS Spine System10705034585383
TRIALTIS Spine System10705034586861
TRIALTIS Spine System10705034586885
TRIALTIS Spine System10705034585352
TRIALTIS Spine System10705034586670
TRIALTIS Spine System10705034586854
TRIALTIS Spine System10705034585628
TRIALTIS Spine System10705034585529
TRIALTIS Spine System10705034585536
TRIALTIS Spine System10705034585307
TRIALTIS Spine System10705034588421
TRIALTIS Spine System10705034585703
TRIALTIS Spine System10705034586892
TRIALTIS Spine System10705034586687
TRIALTIS Spine System10705034585499
TRIALTIS Spine System10705034585093
TRIALTIS Spine System10705034584836
TRIALTIS Spine System10705034589039
TRIALTIS Spine System10705034585291
TRIALTIS Spine System10705034589077
TRIALTIS Spine System10705034589022
TRIALTIS Spine System10705034585284
TRIALTIS Spine System10705034585611
TRIALTIS Spine System10705034585055

1 2 3