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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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Template — 33 UDI-DI variants, MDR

MD Atlas
Sanatmetal Ortopédiai és Traumatológiai Eszközöket Gyártó Kft.

Data from EUDAMED, last updated May 24, 2026

Template

5996527652TEMPLTNSTTZ

33 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: Sanatmetal Ortopédiai és Traumatológiai Eszközöket Gyártó Kft.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 5996527652TEMPLTNSTTZ
Device name: Template
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jan 2, 2024

Manufacturer & authorised representative

Manufacturer

Name: Sanatmetal Ortopédiai és Traumatológiai Eszközöket Gyártó Kft.
SRN: HU-MF-000006772
Country: Hungary
Email: metal@sanatmetal.hu
Phone: +3636512901

Variants by status

UDI-DI variants

33 UDI-DI variants

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Applied filters

basicUdiUlid01HK4RGH0GA8H5YREAKFNT4KJ7

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

Femoral resection template - PS05996527016493
Femoral resection template - PS05996527016486
Femoral resection template - PS05996527026874
Femoral sizer05996527026959
PCL Tibial marking hook05996527048609
Repositioning block05996527027161
Revision cutting block05996527026935
Revision distal resection template05996527023088

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