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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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MMCD LAP F13 10kg — 1 UDI-DI variant, MDD

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

Data from EUDAMED, last updated May 31, 2026

MMCD LAP F13 10kg

B-08588008665565

1 UDI-DI variant

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

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

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Device characteristics

Active device

Legacy certificates

Certificate number: 26007
Type: refdata.legacy.mdd-certificate-type.ii-excluding-4
Notified body: CERTIQUALITY S.r.l. (0546)
Validity: May 26, 2024

Identity & classification

Basic UDI-DI: B-08588008665565
Device name: MMCD LAP F13 10kg
Device model: MMCD LAP F13 10kg
Issuing agency: EUDAMED
Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class IIb
Version date: Apr 11, 2025

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

basicUdiUlid01JRHRZM4B5N3TZA60PY6CDR0S

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

MMCD LAP F13 10kg08588008665565