Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3038129050

FEI Number

3038129050

Entity Name

LAPSI HEALTH

City/State/Country

Amsterdam Noord-Holland, NL

Establishment Address

Matrix One, Unit 1. 53; Science Park 301, Amsterdam Noord-Holland 1098 XH, NL

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Lapsi Health (Owner Number: 10092982)

Owner / Operator Contact Address

Matrix ONE, Science Park 301 unit 1.53, Amsterdam, NL-NH 1098 XH, NL

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K233313

PMA Number

N/A

All Registered Proprietary Names

Keikku

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
DQD	Stethoscope, Electronic	Cardiovascular	Class 2	870.1875	2025-03-13

Official Correspondent

Seamus Holohan

US Agent Details

Dana Burger-Dipzinski Business: Electra-Med Corporation Email: dana@electramed.com Phone: (810) 2324856

Related Public Records

Same Entity

Lapsi Health

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

View Entity Profile →

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K771506	Swartz Medical Equipment	STETHOSCOPE	1977-08-26
K082528	Noble Anesthesia-Air, Inc.	SNOR-SCOPE PLUS OR SNOR-SCOPE + ELECTRONIC STETHOSCOPE SYSTEM	2009-03-06

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3038129050. Last updated year: 2026. Please use registration number 3038129050 when referencing this establishment in official correspondence.