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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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Femoralis-Druckverband — 6 UDI-DI variants, MDR

MD Atlas
Bisping Medizintechnik GmbH

Data from EUDAMED, last updated May 23, 2026

Femoralis-Druckverband

42511143DV5D

6 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: Bisping Medizintechnik GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 42511143DV5D
Device name: Femoralis-Druckverband
Device model: DV100
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 18, 2026

Manufacturer & authorised representative

Manufacturer

Name: Bisping Medizintechnik GmbH
SRN: DE-MF-000006659
Country: Germany
Email: info@bispingmed.de

Variants by status

UDI-DI variants

6 UDI-DI variants

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Applied filters

basicUdiUlid01KRXCF7KDRBE2NKQ5GN7PYSR3

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

0610000304251114300128
0610010304251114300135
0610020304251114300142
0610000104251114300098
0610010104251114300104
0610020104251114300111