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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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N2O cartridges CryoPen — 10 UDI-DI variants, MDR

MD Atlas
H&O Equipments nv/sa

Data from EUDAMED, last updated May 23, 2026

N2O cartridges CryoPen

540700848SHON2OCLN2OUU

10 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: 540700848SHON2OCLN2OUU
Device name: N2O cartridges CryoPen
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Jan 7, 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

10 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KEBXG22DM7EN91BZ36BS6F86

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-NOCX-XL-S0615407008482203
S-HO-NOCX-12-S0625407008482200
CL-N2O-16G-NBOX15407008484214
CL-N2O-16G-NCARTON25407008484211
S-HO-NO23-XX-S0615407008482401
S-HO-NO23-12-S0625407008482408
CL-N2O-35G-BOX15407008484405
CL-N2O-35G-CARTON25407008484402
S-HO-NOCX-12-S2425407008482002
S-HO-NOCX-XX-S2415407008482005