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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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Tube Stool — 6 UDI-DI variants, IVDR (Paul Boettger GmbH & Co. KG)

MD Atlas
Paul Boettger GmbH & Co. KG

Data from EUDAMED, last updated May 23, 2026

Tube Stool

404283607001IVDG7

6 UDI-DI variants

IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]IVDR Class A

Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Manufacturer: Paul Boettger GmbH & Co. KG

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 404283607001IVDG7
Device name: Tube Stool
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: May 6, 2026

Manufacturer & authorised representative

Manufacturer

Name: Paul Boettger GmbH & Co. KG
SRN: DE-MF-000022524
Country: Germany
Email: sales@boettger.com
Phone: +49 9924 9429 0

Variants by status

UDI-DI variants

6 UDI-DI variants

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Applied filters

basicUdiUlid01KQYMRW9AK8MWKGREAA9ZP4N0

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

07-033-200704042836002199
07-011-210104042836002144
07-043-2107-0104042836009013
07-011-200104042836002137
07-023-200704042836002168
07-043-200704042836002229