Loewenstein Medical Technology GMBH + CO. KG

FDA Device Registration & Listing · HAMBURG, DE · Registration 1000537145

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
1000537145
FEI Number
1000537145
Entity Name
Loewenstein Medical Technology GMBH + CO. KG
City/State/Country
HAMBURG, DE
Establishment Address
KRONSAALSWEG 40, HAMBURG 22525, DE
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Loewenstein Medical Technology (Owner Number: 9048414)
Owner / Operator Contact Address
KRONSAALSWEG 40, --, HAMBURG, DE-HH 22525, DE
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

LUISA

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
QOT Emergency Ventilator Unknown Class N N/A 2021-07-20

Official Correspondent

No official correspondent registered.

US Agent Details

Agim Imeri Business: Loewenstein Medical Americas Corp. Email: agim.imeri@lm-americas.com Phone: (404) 6189965

Related Public Records

Same Entity

Loewenstein Medical Technology
View consolidated registration, premarket clearance, and recall records for this applicant.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1000537145. Last updated year: 2026. Please use registration number 1000537145 when referencing this establishment in official correspondence.
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