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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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Medical pendant — 40 UDI-DI variants, MDR (TORUSCARE Sp. z o.o.)

MD Atlas
TORUSCARE Sp. z o.o.

Data from EUDAMED, last updated May 31, 2026

Medical pendant

590218602PENDANTK7

40 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: TORUSCARE Sp. z o.o.

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 590218602PENDANTK7
Device name: —
Device model: Medical pendant
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Aug 11, 2025

Manufacturer & authorised representative

Manufacturer

Name: TORUSCARE Sp. z o.o.
SRN: PL-MF-000047801
Country: Poland
Email: karolina@toruscare.com

Variants by status

UDI-DI variants

40 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01K2BVYJAYGMV0DR870WS62SYR

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

NEXTERA X8105902186022331
NEXTERA X8205902186022386
NEXTERA X9105902186022348
NEXTERA X9205902186022393
NEXTERA XL1205902186022119
NEXTERA XL2105902186022133
NEXTERA XL2205902186022157
NEXTERA XL3105902186022256
NEXTERA XS05902186022294
NEXTERA XX3105902186022201
NEXTERA XX3205902186022171
NEXTERA XX7105902186022324
NEXTERA XX7205902186022379
NEXTERA XXL3105902186022263
NEXTERA XXL3205902186022232

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