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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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PINOFIT Rope pulley — 12 UDI-DI variants, MDR

MD Atlas
PINO Pharmazeutische Präparate GmbH

Data from EUDAMED, last updated May 23, 2026

PINOFIT Rope pulley

426040893SEILZUG31KL

12 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: PINO Pharmazeutische Präparate GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 426040893SEILZUG31KL
Device name: PINOFIT Rope pulley
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jan 6, 2022

Manufacturer & authorised representative

Manufacturer

Name: PINO Pharmazeutische Präparate GmbH
SRN: DE-MF-000005667
Country: Germany
Email: service@pinoshop.com
Phone: +49 40 8997850

Variants by status

UDI-DI variants

12 UDI-DI variants

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Applied filters

basicUdiUlid01FRQ7ADC9AM2XWQVV8PNCG8JV

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

4818704260730021300
4812804260730021294
4818204260408936356
4818104260408935199
601200304260730027999
601200804260730028132
PINOFIT Rope pulley Explosive compact04260730023571
PINOFIT Rope pulley Explosive dark grey04260730024271
PINOFIT Rope pulley Standard dark grey04260730024264
4812904260408936165
4819204260408935281
PINOFIT Vertical lifting device dark grey04260730024288