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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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Guide Wires — 8 UDI-DI variants, MDR (STEMA Medizintechnik GmbH)

MD Atlas
STEMA Medizintechnik GmbH

Data from EUDAMED, last updated Jun 2, 2026

Guide Wires

40492030000089C7

8 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: STEMA Medizintechnik GmbH

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Device characteristics

Reusable

Identity & classification

Basic UDI-DI: 40492030000089C7
Device name: —
Device model: Guide Wires
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 30, 2026

Manufacturer & authorised representative

Manufacturer

Name: STEMA Medizintechnik GmbH
SRN: DE-MF-000005523
Country: Germany
Email: info@stema-medizintechnik.de
Phone: +49 7467 79630 0

Variants by status

UDI-DI variants

8 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KSWJF8YJRZTK04FMZ7TDNXN9

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

Guide Wires04049203212564
Guide Wires04049203219617
Guide Wires04049203212540
Guide Wires04049203219624
Guide Wires04049203219600
Guide Wires04049203212557
Guide Wires04049203219631
Guide Wires04049203212533