PREOMICS GMBH

FDA Device Registration & Listing · Planegg/Martinsried Bavaria, DE · Registration 3013452222

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
3013452222
FEI Number
3013452222
Entity Name
PREOMICS GMBH
City/State/Country
Planegg/Martinsried Bavaria, DE
Establishment Address
Am Klopferspitz 19, Planegg/Martinsried Bavaria 82152, DE
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
PreOmics GmbH (Owner Number: 10061902)
Owner / Operator Contact Address
Am Klopferspitz 19, Planegg/Martinsried, DE-BY 82152, DE
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
PPM General Purpose Reagent Pathology Class 1 864.4010 2019-12-09

Official Correspondent

Garwin Pichler

US Agent Details

Garwin Pichler Email: garwin.pichler@preomics.com Phone: (978) 6633660

Related Public Records

Same Entity

PreOmics GmbH
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 3013452222. Last updated year: 2026. Please use registration number 3013452222 when referencing this establishment in official correspondence.
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