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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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Momosan clima — 13 UDI-DI variants, MDR (Moltoplast GmbH)

MD Atlas
Moltoplast GmbH

Data from EUDAMED, last updated May 23, 2026

Momosan clima

900601862999A6

13 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class I

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: Moltoplast GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 900601862999A6
Device name: Momosan clima
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Feb 15, 2022

Manufacturer & authorised representative

Manufacturer

Name: Moltoplast GmbH
SRN: AT-MF-000004503
Country: Austria
Email: med@moltoplast.com
Phone: +43 512 585407

Variants by status

UDI-DI variants

13 UDI-DI variants

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Applied filters

basicUdiUlid01FVHNF0WXGTY3SZSHVAFD85CV

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

6170590060186170570
61608-290060186080244
6170290060186170266
6178090060186178040
6160690060186160670
6170390060186170334
6161490060186161424
6170790060186170716
6170190060186170198
6170490060186170402
6170590060186170570
6170690060186170648
6170890060186170884