Pricing Sign in

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Partners Contact

Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

Haube und Beutel — 31 UDI-DI variants, MDR

MD Atlas
Udo Heisig GmbH The Disposables Company

Data from EUDAMED, last updated May 23, 2026

Haube und Beutel

42518062005L6

31 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: Udo Heisig GmbH The Disposables Company

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 42518062005L6
Device name: Haube und Beutel
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 19, 2025

Manufacturer & authorised representative

Manufacturer

Name: Udo Heisig GmbH The Disposables Company
SRN: DE-MF-000009334
Country: Germany
Email: info@heisig.de
Phone: 0894623920

Variants by status

UDI-DI variants

31 UDI-DI variants

Sign in to export

Exports are reserved for signed-in users. Sign in or create an account to continue.

Email

Password

No account yet?

Export results

Applied filters

basicUdiUlid01JVKWS4AVDJ8Q2XFCWHSV4XEZ

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

3140004251806200361
3020004251806200194
3006504251806200088
3010004251806202709
3004504251806200064
3018004251806200170
3016004251806200163
3025004251806200217
3008504251806200118
3008604251806200125
3006104251806200071
3007704251806200095
3007904251806200101
3009604251806200149
3009404251806200132
3074104251806200279
3079104251806200286
3814004251806201092
3812504251806201085
3808004251806201054
3810004251806201061
3811004251806201078
3802504251806201009
3806004251806201030
3803004251806201016

1 2