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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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CloudCuddle_hoes — 3 UDI-DI variants, MDR (CloudCuddle)

MD Atlas
CloudCuddle

Data from EUDAMED, last updated May 30, 2026

CloudCuddle_hoes

8719326288CC-J93

3 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: CloudCuddle

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 8719326288CC-J93
Device name: CloudCuddle_hoes
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jan 13, 2023

Manufacturer & authorised representative

Manufacturer

Name: CloudCuddle
SRN: NL-MF-000010952
Country: Netherlands
Email: info@humanprotection.nl
Phone: +31135363807

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01GF0HB0ZHV751P4JZSHDEQ9S0

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

Inflatable frame08719326288888
Sheet08719326288871
0608719326288895