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.

RIDASCREEN® Entamoeba — 5 UDI-DI variants, IVDR (R-Biopharm AG)

MD Atlas
R-Biopharm AG

Data from EUDAMED, last updated May 23, 2026

RIDASCREEN® Entamoeba

4049095C170100000KM

5 UDI-DI variants

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

Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class B
Manufacturer: R-Biopharm AG

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

ReagentProfessional testingAnimal tissues / cells

Clinical investigations

Registered: No

Identity & classification

Basic UDI-DI: 4049095C170100000KM
Device name: RIDASCREEN® Entamoeba
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class B
Version date: Dec 5, 2022

Manufacturer & authorised representative

Manufacturer

Name: R-Biopharm AG
SRN: DE-MF-000007993
Country: Germany
Email: t.zeugfang@r-biopharm.de

Variants by status

UDI-DI variants

5 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

basicUdiUlid01GK6JEM1HEGQWPX58M0SAW8T9

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

C1701C01-VK04049095030727
C170104049095030086
C1701K02-VK04049095030741
C1701K01-VK04049095030734
CRP170404049095030239