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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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Argon med. Messer 15,3m3 F50 P300 — 1 UDI-DI variant, MDD

MD Atlas
Messer Tatragas, spol. s r.o.

Data from EUDAMED, last updated May 30, 2026

Argon med. Messer 15,3m3 F50 P300

B-08588008665367

1 UDI-DI variant

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

Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class I
Manufacturer: Messer Tatragas, spol. s r.o.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: B-08588008665367
Device name: Argon med. Messer 15,3m3 F50 P300
Device model: Argon med. Messer 15,3m3 F50 P300
Issuing agency: EUDAMED
Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class I
Version date: Jun 30, 2023

Manufacturer & authorised representative

Manufacturer

Name: Messer Tatragas, spol. s r.o.
SRN: SK-MF-000027886
Country: Slovakia
Email: jana.nemethova@messergroup.com
Phone: +421250254111

Variants by status

UDI-DI variants

1 UDI-DI variant

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Applied filters

basicUdiUlid01H45Q078G4ZBH9XZ2TWPM1MEK

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

Argon med. Messer 15,3m3 F50 P30008588008665367