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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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Teleskopstock 150 — 4 UDI-DI variants, MDR

MD Atlas
Kellerer Blindenstöcke e.K. Inh. Gerhard Koneberg

Data from EUDAMED, last updated May 23, 2026

Teleskopstock 150

42700052504001BL

4 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: Kellerer Blindenstöcke e.K. Inh. Gerhard Koneberg

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 42700052504001BL
Device name: Teleskopstock 150
Device model: T150
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 24, 2026

Manufacturer & authorised representative

Manufacturer

Name: Kellerer Blindenstöcke e.K. Inh. Gerhard Koneberg
SRN: DE-MF-000049808
Country: Germany
Email: info@kellerer-blindenstoecke.de

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01KMFXCNEZEND37WWT752EVPHR

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

T15004270005250403
T14004270005250434
DT14542700052504278
T12504270005250410