Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3014383580

FEI Number

3014383580

Entity Name

TRIPLE A MARKETING GMBH

City/State/Country

Bielefeld North Rhine-Westphalia, DE

Establishment Address

Am Lenkwerk 3, Bielefeld North Rhine-Westphalia 33609, DE

Establishment Type(s)

Export Device to the United States But Perform No Other Operation on Device

Owner / Operator

Triple A Marketing GMBH (Owner Number: 10083317)

Owner / Operator Contact Address

Am Lenkwerk 3, Bielefeld, DE-NOTA 33609, DE

Initial Importer Flag

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
HHE	Cup, Menstrual	Obstetrics/Gynecology	Class 2	884.5400	2021-11-10

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

Triple A Marketing GMBH

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

View Entity Profile →

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3010965020	meluna	Haundorf Bavaria, DE

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3014383580. Last updated year: 2026. Please use registration number 3014383580 when referencing this establishment in official correspondence.