Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3033436415

FEI Number

3033436415

Entity Name

STARBIA MEDITEK CO., LTD.

City/State/Country

Taichung City, TW

Establishment Address

3rd Floor, No. 159-1, Sec. 1, Zhongxing Road, Dali District, Taichung City 41267, TW

Establishment Type(s)

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

Owner / Operator

Starbia Meditek Co., Ltd. (Owner Number: 10091421)

Owner / Operator Contact Address

3rd Floor, No. 159-1, Sec. 1, Zhongxing Road, Dali District, Taichung City, TW-TXG 41267, TW

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

SA-701, SA-201

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
PUH	Analyzer, Body Composition, Exempt	Cardiovascular	Class 2	870.2770	2024-10-03

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

Starbia Meditek Co., Ltd.

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 3033436415. Last updated year: 2026. Please use registration number 3033436415 when referencing this establishment in official correspondence.