AEROPHARM GmbH

FDA Device Registration & Listing · Rudolstadt Thuringia, DE · Registration 3005831843

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
3005831843
FEI Number
3005831843
Entity Name
AEROPHARM GmbH
City/State/Country
Rudolstadt Thuringia, DE
Establishment Address
Francois-Mitterrand-Allee 1, Rudolstadt Thuringia D-07407, DE
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Sandoz Inc (Owner Number: 10046594)
Owner / Operator Contact Address
100 College Road West, Princeton, NJ 08540, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K124026
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
KZH Introducer, Syringe Needle General Hospital Class 2 880.6920 2014-04-11

Official Correspondent

Gregory Seitz

US Agent Details

Gregory Seitz Business: SANDOZ INC Email: gregory.seitz@sandoz.com Phone: (609) 4224162

Related Public Records

Same Entity

Sandoz Inc
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 3005831843. Last updated year: 2026. Please use registration number 3005831843 when referencing this establishment in official correspondence.
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