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

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VERSALOK Ti Anchor — 2 UDI-DI variants, MDR (Medos International SARL)

MD Atlas
Medos International SARL

Data from EUDAMED, last updated May 23, 2026

VERSALOK Ti Anchor

0886705a00092KN

2 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

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Device characteristics

Implantable

Identity & classification

Basic UDI-DI: 0886705a00092KN
Device name: VERSALOK Ti Anchor
Device model: VERSALOK Ti
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: Oct 7, 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

2 UDI-DI variants

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Applied filters

basicUdiUlid01K702ND13BHBS91BG9HDNK0Q8

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

VERSALOK ANCHOR10886705001163
VERSALOK ANCHOR W/ORTHOCORD10886705001224