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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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Carrelli emergenza Serie Krazy -… — 6 UDI-DI variants, MDR

MD Atlas
KARREL HEALTH SOLUTIONS SRL

Data from EUDAMED, last updated May 31, 2026

Carrelli emergenza Serie Krazy - K82026XX

805969385K82026XXKJ

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: KARREL HEALTH SOLUTIONS SRL

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 805969385K82026XXKJ
Device name: Carrelli emergenza Serie Krazy - K82026XX
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 20, 2026

Manufacturer & authorised representative

Manufacturer

Name: KARREL HEALTH SOLUTIONS SRL
SRN: IT-MF-000028683
Country: Italy
Email: info@karrel.it
Phone: 05221750501

Variants by status

UDI-DI variants

6 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KS2W4W3ZKFR2WNJT2Z4FCMFA

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

K820261X08059693850203
K820262X08059693850227
K82026108059693850197
K82026208059693850210
K820260X08059693850180
K82026008059693850173