Statistics for BIOEUROPE GmbH

18Total Devices

18Basic UDI-DIs

0Not destined for EU market

0Certificates

0Valid

0Expiring < 6 months

1Countries

Certificate health for BIOEUROPE GmbH

No certificates registered for this manufacturer.

Showing 1–18 of 18 devices.

Trade name	Reference / catalog number	UDI-DI code	Quantity	Status
Bioeurope 14 Food Intolerance Test (ref:7182)	`7182`	`D-7182BH`	1	On the market
Bioeurope 14 Food Intolerance Test (ref:7194)	`7194`	`42623675671946`	1	On the market
Bioeurope 4 Food Intolerance Test (ref:7184)	`7184`	`D-7184BM`	1	On the market
Bioeurope 4 Food Intolerance Test (ref:7187)	`7187`	`D-7187BT`	1	On the market
Bioeurope 42 Food Intolerance Test (ref:7179)	`7179`	`42623675671793`	1	On the market
Bioeurope 7 Food Intolerance Test (ref:7181)	`7181`	`D-7181BF`	1	On the market
Bioeurope 7 Food Intolerance Test (ref:7189)	`7189`	`42623675671892`	1	On the market
Bioeurope 90 Food Intolernace Test (ref:7180)	`7180`	`D-7180BD`	1	On the market
EZ-Microalbumin Screening Test	`1400-25`	`42623675614257`	1	On the market
Fortel Kidney Disease (Microalbumin) Screening Test	`1400-1`	`D-1400-1L9`	1	On the market
Fortel Prostate (PSA) Screening Test	`1081-1`	`D-1081-1LS`	1	On the market
Fortel Ulcer (H. pylori) Screening Test	`1005-1`	`D-1005-1KN`	1	On the market
Fortel Ultra Sensitive Pregnancy Midstream 1-Test	`1147-02`	`42623675614721`	1	On the market
Fortel Ultra Sensitive Pregnancy Midstream 1-Test	`1147-01`	`D-1147-01V2`	1	On the market
Isletest GAD ELISA	`7009`	`D-7009B2`	1	On the market
Isletest IAA ELISA	`7011`	`D-7011AM`	1	On the market
Isletest ICA ELISA	`7010`	`D-7010AK`	1	On the market
NutriDetect 90G B ELISA	`7180`	`42623675671809`	3	On the market

Devices placed in 1 country

EUDAMED update: May 14, 2026

DE-MF-000039230

Active

BARKOW Tom
Person Responsible for Regulatory Reporting under Articles 82–86 and Post-Market Surveillance Compliance under Article 10(10).
Hidden
QIU Bonnie
Person Responsible for for Device Conformity Verification, Technical Documentation Oversight, Post-Market Surveillance Compliance under Article 10(9), and Investigational Device Statements.
Hidden