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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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SBM 22 — 3 UDI-DI variants, MDR (Hans Dinslage GmbH)

MD Atlas
Hans Dinslage GmbH

Data from EUDAMED, last updated May 23, 2026

SBM 22

4066299SBM22WF

3 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIa

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: Hans Dinslage GmbH

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Device characteristics

Active deviceMeasuring function

Identity & classification

Basic UDI-DI: 4066299SBM22WF
Device name: —
Device model: SBM 22
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Mar 20, 2025

Manufacturer & authorised representative

Manufacturer

Name: Hans Dinslage GmbH
SRN: DE-MF-000005488
Country: Germany
Email: service@sanitas-online.de

Variants by status

UDI-DI variants

3 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01JPS7PQVQDH9TCBVKZ5YK1YVY

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

1006404066299100643
1006204066299100629
6095304066299609535