NeoPredics AG

FDA Device Registration & Listing · Regensburg Bavaria, DE · Registration 3020521802

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3020521802
FEI Number
3020521802
Entity Name
NeoPredics AG
City/State/Country
Regensburg Bavaria, DE
Establishment Address
Franz-Mayer-Strasse 1, Regensburg Bavaria 93053, DE
Establishment Type(s)
Manufacture Medical Device,Complaint File Establishment per 21 CFR 820.198
Owner / Operator
NeoPrediX AG (Owner Number: 10082724)
Owner / Operator Contact Address
Franz-Mayer-Strasse 1, Regensburg, DE-BY 93053, DE
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

BiliPredics

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
PQQ Data Acquisition Software Clinical Chemistry Class 2 862.2570 2021-09-23

Official Correspondent

No official correspondent registered.

US Agent Details

Thorsten Waloschek Email: thorsten.waloschek@neopredix.com Phone: (908) 9389114

Related Public Records

Same Entity

NeoPrediX AG
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3020521802. Last updated year: 2026. Please use registration number 3020521802 when referencing this establishment in official correspondence.
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