Keikku Digital Stethoscope KEIKKUGEN1

by Lapsi Health Holding B.V. GUDID

Listed FDA GUDID listing, no authorization on record

Regulatory status

as of 29 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number06429811134003 UDI-DI	Date16 Oct 2025Listed	StatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Recalls

0 recalls · FDA

No FDA recalls on record, checked 22 Oct 2026.

Specification

GUDID

Trade Name: Keikku Digital Stethoscope
Generic Name: Electronic acoustic stethoscope
Model / Reference: KEIKKUGEN1

Primary DI / UDI-DI: 06429811134003
510(k) Number: K233313
FDA Product Code: DQD
GMDN Term: Electronic acoustic stethoscope

Device Class: Class II
Regulation Number: 870.1875
GUDID distribution status: In Commercial Distribution

Other devices from Lapsi Health Holding B.V.

Keikku Scribe

Class I
Keikku Electronic stethoscope

Class II

Properties

Prescription Use
Lot / Batch Number
Serial Number
Manufacturing Date

Other properties (10)

Sterile: No
Single Use: No
Implantable: No
Contains Latex: No
Over-the-Counter: No
Convenience Kit: No
Combination Product: No
HCT/P: No
Premarket Exempt: No
Expiration Date: No