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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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Secretion jar — 3 UDI-DI variants, MDR

MD Atlas
Heinemann HNO Medizintechnik GmbH

Data from EUDAMED, last updated May 23, 2026

Secretion jar

0426251221SEJWE

3 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: Heinemann HNO Medizintechnik GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 0426251221SEJWE
Device name: Secretion jar
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 22, 2026

Manufacturer & authorised representative

Manufacturer

Name: Heinemann HNO Medizintechnik GmbH
SRN: DE-MF-000046391
Country: Germany
Email: info@heinemann-ent.de
Phone: +49 4191 95 379 0

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01KPTTAJNKE0VK878J8JQNF3RZ

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

Secretion jar -04262512210490
Secretion jar - complete04262512210476
Secretion jar - lid04262512210483