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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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PADSY Spiro — 4 UDI-DI variants, MDR (Medset Medizintechnik GmbH)

MD Atlas
Medset Medizintechnik GmbH

Data from EUDAMED, last updated May 23, 2026

PADSY Spiro

42504037AAG147000-00D6

4 UDI-DI variants

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

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

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Device characteristics

Active deviceMeasuring function

Identity & classification

Basic UDI-DI: 42504037AAG147000-00D6
Device name: PADSY Spiro
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Special device type: refdata.special-mdr-device-type.software
Version date: Apr 20, 2026

Manufacturer & authorised representative

Manufacturer

Name: Medset Medizintechnik GmbH
SRN: DE-MF-000016442
Country: Germany
Email: h.madlung@medset.com
Phone: 0407258220

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01JFAHDTR54WW29QF1VAF86KZN

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

AAG14710104250403740027
AAG14710104250403740034
AAG14710204250403740041
AAG14710304250403740058