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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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CryoPen — 9 UDI-DI variants, MDR (H&O Equipments nv/sa)

MD Atlas
H&O Equipments nv/sa

Data from EUDAMED, last updated May 23, 2026

CryoPen

540700848SHOCPECLFP8G

9 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIa

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: H&O Equipments nv/sa

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 540700848SHOCPECLFP8G
Device name: CryoPen
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Apr 23, 2026

Manufacturer & authorised representative

Manufacturer

Name: H&O Equipments nv/sa
SRN: BE-MF-000000992
Country: Belgium
Email: info@ho-equipments.com
Phone: +3268268600

Variants by status

UDI-DI variants

9 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01JD27YM3VFFV0K9B8WDWH12M3

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

S-HO-CBPLUS-0615407008480216
S-HO-CMPE-0115407008480018
S-HO-COPE-0215407008480315
S-HO-CXPEP-0215407008480117
S-HO-CEPE-0115407008480513
S-HO-CEPEPLUS-0015407008480520
S-HO-CESPE-0015407008480704
CL-FP-1915407008483217
CL-FP-3615407008483415