Pricing Sign in

Role
Country
Date of registration
Address

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Contact

Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

Organization name
UDI-DI code
Reference / catalog number

303106022 — Class IIa MDD by Messer Industriegase GmbH

MD Atlas
Messer Industriegase GmbH

EUDAMED last updated this device on Mar 14, 2023

303106022

B-04262389120144

On the marketClass IIa

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: Messer Industriegase GmbH
UDI-DI code: 04262389120144
Reference / catalog number: 303106022

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

Manufacturer information

Organization name: Messer Industriegase GmbH
SRN: DE-MF-000016610
Manufacturer status: Active

Related devices

300182032426238912MIGG018MOn the market 303100202B-04262389120359On the market 303100142B-04262389120342On the market 303100012B-04262389120267On the market 103106122B-04262389120533On the market

Certificates

No certificates registered for this manufacturer.

No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.

Market distribution

Primary placement in Germany; available across 1 country total.

Country	On market since	Until
GermanyPrimary placement	Dec 20, 2018	Still on market

Device identification

Trade name: not provided
UDI-DI code: 04262389120144
Basic UDI-DI: B-04262389120144
Reference / catalog number: 303106022
Issuing entity: GS1

Classification

Risk category: Class IIa
Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: 2L (1,5kg), Kundeneigentum, ALU, Steigrohr
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

V0901CLINICAL/THERAPEUTIC APPLICATIONS CARBON DIOXIDE

Compliance flags

Safety

Sterile

Single use

Contains latex

Reprocessed single-use

Direct marking

Substances

CMR substance

Endocrine disruptor

Regulatory

Annex XVI applicable

Sterilization

Lifecycle

New device

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification