MEDIFUN CORPORATION

FDA Device Registration & Listing · Taichung, TW · Registration 3002680783

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3002680783
FEI Number
3002680783
Entity Name
MEDIFUN CORPORATION
City/State/Country
Taichung, TW
Establishment Address
4F-1, 4F-9, 4F-10, No.99, Jingke S. Rd., Nantun Dist.,, Taichung 40818, TW
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
Medifun Corporation (Owner Number: 10050917)
Owner / Operator Contact Address
4F-1, 4F-9, 4F-10, No.99, Jingke S. Rd., Nantun Dist.,, Taichung, TW-TXG 40818, TW
Initial Importer Flag
N
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
QRL Multiple Use Blood Lancet For Single Patient Use Only General, Plastic Surgery Class 2 878.4850 2024-03-18

Official Correspondent

Jamie Tsai

US Agent Details

David Lee Business: Dynamic Biotech, Inc. Email: davidlee@ivddreg.com Phone: (949) 2180929

Related Public Records

Same Entity

Medifun Corporation
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 3002680783. Last updated year: 2026. Please use registration number 3002680783 when referencing this establishment in official correspondence.
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