Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3042024535

FEI Number

3042024535

Entity Name

PT YOUMI MEDIKA INDUSTRI

City/State/Country

Batang Sulawesi Utara, ID

Establishment Address

Akasia Street Unit A-24, A-25, A-26, A-27, A-28, A-29, Kedawung Subdistrict, Banyuputih District, Batang Sulawesi Utara 51271, ID

Establishment Type(s)

Manufacture Medical Device,Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

PT Youmi Medika Industri (Owner Number: 10094827)

Owner / Operator Contact Address

Akasia Street Unit A-24, A-25, A-26, A-27, A-28, A-29, Kedawung Subdistrict, Banyuputih District, Batang, ID-NOTA 51271, ID

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Solvent, adhesive tape-Adhesive Remover Pad Pad, Alcohol Prep Pad, device disinfectant

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
KOX	Solvent, Adhesive Tape	General, Plastic Surgery	Class 1	878.4730	2025-12-26
LKB	Pad, Alcohol, Device Disinfectant	Unknown	Class U	N/A	2026-01-02

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

PT Youmi Medika Industri

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

View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3042024535. Last updated year: 2026. Please use registration number 3042024535 when referencing this establishment in official correspondence.