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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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Rasps, Other — 41 UDI-DI variants, MDR (STEMA Medizintechnik GmbH)

MD Atlas
STEMA Medizintechnik GmbH

Data from EUDAMED, last updated May 31, 2026

Rasps, Other

40492030000043BF

41 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

41 UDI-DI variants

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Applied filters

basicUdiUlid01KSTABS8YF5YAVB7YEB37V7F3

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

Rasps, Other04049203064804
Rasps, Other04049203093590
Rasps, Other04049203135252
Rasps, Other04049203147842
Rasps, Other04049203064811
Rasps, Other04049203103428
Rasps, Other04049203093675
Rasps, Other04049203169622
Rasps, Other04049203064781
Rasps, Other04049203093606
Rasps, Other04049203093682
Rasps, Other04049203110051
Rasps, Other04049203169615
Rasps, Other04049203111911
Rasps, Other04049203093705
Rasps, Other04049203111560
Rasps, Other04049203093613
Rasps, Other04049203093651
Rasps, Other04049203132596
Rasps, Other04049203093644
Rasps, Other04049203093576
Rasps, Other04049203130226
Rasps, Other04049203064750
Rasps, Other04049203064774
Rasps, Other04049203147859

1 2

Device characteristics

Reusable

Identity & classification

Basic UDI-DI: 40492030000043BF
Device name: —
Device model: Rasps, 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