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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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Bender — 6 UDI-DI variants, MDR (MEDIN, a.s.)

MD Atlas
MEDIN, a.s.

Data from EUDAMED, last updated May 23, 2026

Bender

85917125170721Y6

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: MEDIN, a.s.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 85917125170721Y6
Device name: Bender
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 15, 2026

Manufacturer & authorised representative

Manufacturer

Name: MEDIN, a.s.
SRN: CZ-MF-000012371
Country: Czechia
Email: oldrich.pospichal@medin.cz
Phone: +420566684218

Variants by status

UDI-DI variants

6 UDI-DI variants

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Applied filters

basicUdiUlid01KP8JX77GMFSVDDJ27XG12Q20

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

Bender; fissure-type, 90°08591712279638
Bender; fissure-type, straight08591712279645
Bender; pin-type, 40°08591712286711
Bender; pin-type, straight08591712237348
Bender; universal, type A08591712402418
Bender; universal, type B08591712402425