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.

TLX Implant — 152 UDI-DI variants, MDR (Institut Straumann AG)

MD Atlas
Institut Straumann AG

Data from EUDAMED, last updated May 23, 2026

TLX Implant

0763003170095R7

152 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: Institut Straumann AG

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: 0763003170095R7
Device name: TLX Implant
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: Jan 25, 2026

Manufacturer & authorised representative

Manufacturer

Name: Institut Straumann AG
SRN: CH-MF-000009933
Country: Switzerland
Email: info@straumann.com
Phone: +41 61 965 11 11

Authorised representative

Name: Etkon GmbH
SRN: DE-AR-000009335
Country: Germany
Phone: +49 89 30 90 75-0

Variants by status

UDI-DI variants

152 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

basicUdiUlid01KFTJRWK2QHMNGPPY052YD8H9

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

035.3108S07630031742773
035.2518S07630031742537
035.0006S07630031752093
035.1118S07630031752000
035.0518S07630031751782
035.2118S07630031742254
035.2116S07630031742247
035.3712S07630031743213
035.1016S07630031751928
035.3414S07630031743015
035.3204S07630031755568
035.1008S07630031751881
035.1708S07630031752024
035.3412S07630031743008
035.0416S07630031751706
035.3812S07630031743251
035.1408S07630031751249
035.1510S07630031751324
035.0106S07630031752161
035.3410S07630031742995
035.2512S07630031742506
035.2114S07630031742230
035.0114S07630031752208
035.1010S07630031751898
035.3418S07630031743039

1 2 3 4 5