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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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INSTRUMENTS — 5 UDI-DI variants, MDR (Surgi-Tec NV)

MD Atlas
Surgi-Tec NV

Data from EUDAMED, last updated May 23, 2026

INSTRUMENTS

540700775INSTBW

5 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: Surgi-Tec NV

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 540700775INSTBW
Device name: INSTRUMENTS
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Aug 16, 2022

Manufacturer & authorised representative

Manufacturer

Name: Surgi-Tec NV
SRN: BE-MF-000000257
Country: Belgium
Email: info@surgi-tec.com
Phone: +32 (0)92300569

Variants by status

UDI-DI variants

5 UDI-DI variants

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Applied filters

basicUdiUlid01G7V9CK5FJB43ZCGYZFG019RX

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

TPD All-In-One / Classic - Patient Key05407007750931
TPD All-In-One / Classic Dummies05407007750955
TPD NEO - Patient Key05407007750689
TPD NEO – Patient Hinged Key05407007753369
TPD NEO Dummies05407007750702