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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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SAUER-Sportbeutel - steril — 8 UDI-DI variants, MDR

MD Atlas
Manfred Sauer GmbH

Data from EUDAMED, last updated May 23, 2026

SAUER-Sportbeutel - steril

42502745000009EQ

8 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: Manfred Sauer GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 42502745000009EQ
Device name: SAUER-Sportbeutel - steril
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Nov 24, 2025

Manufacturer & authorised representative

Manufacturer

Name: Manfred Sauer GmbH
SRN: DE-MF-000006287
Country: Germany
Email: info@manfred-sauer.de
Phone: +49 6226 960 100

Variants by status

UDI-DI variants

8 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KAV4HN6ED3SQRQ5J2TKK7M3R

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

721.3720.S04250274546575
721.3720.SE04250274527604
721.3730.SE04250274539089
721.3730.S04250274546636
721.1720.S04250274513959
721.1720.SE04250274515595
721.1730.SE04250274515588
721.1730.S04250274513973