Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3002818647

FEI Number

3002818647

Entity Name

AEROLITE AG

City/State/Country

Ennetburgen Nidwalden, CH

Establishment Address

Aumuhlestrasse 10, Ennetburgen Nidwalden CH-6373, CH

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Aerolite AG (Owner Number: 10062144)

Owner / Operator Contact Address

Aumuhlestrasse 10, Ennetburgen, CH-NW CH-6373, CH

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Stars H145 P/N: 145-0262772-501 Stretcher P/N:005-0070301; P/N:005-0070302; P/N: 005-0262771-501 Stretcher AB 139 P/N:005_059 Stretcher Cirrus P/N: CI-2010-321-00

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
FPO	Stretcher, Wheeled	General Hospital	Class 2	880.6910	2019-12-23
NZD	Stretcher, Patient Restraint	General Hospital	Class 1	880.6900	2019-12-23

Official Correspondent

No official correspondent registered.

US Agent Details

David Lennarz Business: Registrar Corp Email: david.lennarz@registrarcorp.com Phone: (757) 2240177

Related Public Records

Same Entity

Aerolite AG

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0023-05	Stryker Medical	2	Stryker brand Rugged EZ-Pro R4 Ambulance Cot, model 6092.

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3003674698	MedSource Labs, LLC	Chanhassen, MN, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3002818647. Last updated year: 2026. Please use registration number 3002818647 when referencing this establishment in official correspondence.