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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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CARBON DIOXIDE (MEDICAL DEVICE) 2.5L — 1 UDI-DI variant, MDD

MD Atlas
Linde Sverige AB (Linde Gas)

Data from EUDAMED, last updated May 30, 2026

CARBON DIOXIDE (MEDICAL DEVICE) 2.5L

B-07350114048072

1 UDI-DI variant

MDD [Directive 93/42/EEC on medical devices]Class IIa

Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class IIa
Manufacturer: Linde Sverige AB (Linde Gas)

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Device characteristics

Active device

Legacy certificates

Certificate number: DD 2349717-1
Type: refdata.legacy.mdd-certificate-type.v
Notified body: TÜV Rheinland LGA Products GmbH (0197)
Validity: Jan 16, 2024

Identity & classification

Basic UDI-DI: B-07350114048072
Device name: CARBON DIOXIDE (MEDICAL DEVICE) 2.5L
Issuing agency: EUDAMED
Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class IIa
Version date: May 18, 2022

Manufacturer & authorised representative

Manufacturer

Name: Linde Sverige AB (Linde Gas)
SRN: SE-MF-000004424
Country: Sweden
Email: kundservice.se@linde.com
Phone: 0738432546

Variants by status

UDI-DI variants

1 UDI-DI variant

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Applied filters

basicUdiUlid01G35Z5VDV6NF1DP4VFCTVM860

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

CARBON DIOXIDE (MEDICAL DEVICE) 2.5L07350114048072