Bingli's
Instructions for Use (IFU) - Bingli's Dynamic Anamnesis Module
The electronic Instructions for Use (eIFU) for the Dynamic Anamnesis Module are provided in electronic format in accordance with Regulation (EU) 2017/745 and Commission Implementing Regulation (EU) 2021/2226. The latest approved version, including revision status, is accessible via this website. A paper version of the Instructions for Use may be requested free of charge by contacting info@mybingli.com. Upon receipt of a request, a paper copy will be provided within 7 calendar days and delivered by regular mail. The Dynamic Anamnesis Module is a CE-marked medical device compliant with Regulation (EU) 2017/745 (MDR). The software is intended to support healthcare professionals by structuring and standardising patient-reported information within clinician-controlled workflows. Outputs are informational and non-binding and require professional review and validation. The device does not independently determine diagnoses, triage outcomes, or clinical decisions.
Information provided on this website is for informational purposes only and does not replace the official Instructions for Use or Declaration of Conformity. Users shall always consult the current approved IFU prior to use.
Manufacturer: Bingli NV
Lange Gasthuisstraat 29
2000 Antwerp – Belgium
Single Registration Number (SRN): BE-MF-000040225
Lange Gasthuisstraat 29
2000 Antwerp – Belgium
Single Registration Number (SRN): BE-MF-000040225
Version 3.0 (DE)
Datum der ersten Veröffentlichung: Mai 2024
Deutsche Version herunterladen (pdf Format)Version 3.0 (NL)
Eerste datum van schrijven: Mei 2024
Nederlandstalige versie downloaden (pdf formaat)