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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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Chisels, Other — 60 UDI-DI variants, MDR (STEMA Medizintechnik GmbH)

MD Atlas
STEMA Medizintechnik GmbH

Data from EUDAMED, last updated May 31, 2026

Chisels, Other

40492030000028BK

60 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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UDI-DI variants

60 UDI-DI variants

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Applied filters

basicUdiUlid01KST5CZPQAA568T4FCKWT97XJ

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

Chisels, Other04049203110785
Chisels, Other04049203065016
Chisels, Other04049203157957
Chisels, Other04049203158541
Chisels, Other04049203085175
Chisels, Other04049203157926
Chisels, Other04049203085052
Chisels, Other04049203064941
Chisels, Other04049203158534
Chisels, Other04049203110525
Chisels, Other04049203158473
Chisels, Other04049203157919
Chisels, Other04049203085083
Chisels, Other04049203158442
Chisels, Other04049203065092
Chisels, Other04049203085144
Chisels, Other04049203065108
Chisels, Other04049203085045
Chisels, Other04049203064958
Chisels, Other04049203085106
Chisels, Other04049203108331
Chisels, Other04049203085076
Chisels, Other04049203065047
Chisels, Other04049203110778
Chisels, Other04049203169417

1 2 3

Device characteristics

Reusable

Identity & classification

Basic UDI-DI: 40492030000028BK
Device name: —
Device model: Chisels, Other
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 29, 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