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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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Forceps, Other — 397 UDI-DI variants, MDR (STEMA Medizintechnik GmbH)

MD Atlas
STEMA Medizintechnik GmbH

Data from EUDAMED, last updated Jun 2, 2026

Forceps, Other

40492030000125BJ

397 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

397 UDI-DI variants

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Applied filters

basicUdiUlid01KSWMFR71GPMEJV4TP7F7AW9B

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

Forceps, Other04049203120951
Forceps, Other04049203167482
Forceps, Other04049203167352
Forceps, Other04049203079884
Forceps, Other04049203143592
Forceps, Other04049203209588
Forceps, Other04049203184700
Forceps, Other04049203120937
Forceps, Other04049203023740
Forceps, Other04049203009799
Forceps, Other04049203106498
Forceps, Other04049203145190
Forceps, Other04049203183550
Forceps, Other04049203154666
Forceps, Other04049203142939
Forceps, Other04049203143387
Forceps, Other04049203211970
Forceps, Other04049203064293
Forceps, Other04049203167413
Forceps, Other04049203107433
Forceps, Other04049203063623
Forceps, Other04049203160384
Forceps, Other04049203108485
Forceps, Other04049203145138
Forceps, Other04049203006699

1 2 3 4 5

Device characteristics

Reusable

Identity & classification

Basic UDI-DI: 40492030000125BJ
Device name: —
Device model: Forceps, Other
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