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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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Hooks, Other — 39 UDI-DI variants, MDR (STEMA Medizintechnik GmbH)

MD Atlas
STEMA Medizintechnik GmbH

Data from EUDAMED, last updated May 31, 2026

Hooks, Other

40492030000035BG

39 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

39 UDI-DI variants

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Applied filters

basicUdiUlid01KST78B8FQBA6D44B1EPTFBS3

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

Hooks, Other04049203215619
Hooks, Other04049203088664
Hooks, Other04049203108614
Hooks, Other04049203093736
Hooks, Other04049203147644
Hooks, Other04049203064910
Hooks, Other04049203093767
Hooks, Other04049203088671
Hooks, Other04049203147538
Hooks, Other04049203216401
Hooks, Other04049203215701
Hooks, Other04049203170154
Hooks, Other04049203130257
Hooks, Other04049203216395
Hooks, Other04049203170147
Hooks, Other04049203088695
Hooks, Other04049203108621
Hooks, Other04049203215695
Hooks, Other04049203121569
Hooks, Other04049203208253
Hooks, Other04049203215633
Hooks, Other04049203133494
Hooks, Other04049203093750
Hooks, Other04049203169806
Hooks, Other04049203131377

1 2

Device characteristics

Reusable

Identity & classification

Basic UDI-DI: 40492030000035BG
Device name: —
Device model: Hooks, 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