Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3006979803

FEI Number

3006979803

Entity Name

CHI FENG CO.,LTD

City/State/Country

New Taipei City, TW

Establishment Address

No.11, Ln. 15, Sec. 2, Jiayuan Rd., Shulin Dist.,, New Taipei City 23850, TW

Establishment Type(s)

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

Owner / Operator

CHI FENG CO.,LTD (Owner Number: 10025211)

Owner / Operator Contact Address

No.11, Ln. 15, Sec. 2, Jiayuan Rd.,, Shulin Dist., New Taipei, TW-TPE 23880, TW

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

AiroPur BFC Mojo Recon Direct Vial Access Bag Spike; Vial Direct to Bag (VDB) Sand Trap

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
EHZ	Evacuator, Oral Cavity	Dental	Class 1	872.6640	2020-10-08
EID	Syringe, Restorative And Impression Material	Dental	Class 1	872.4565	2008-03-25
LHI	Set, I.V. Fluid Transfer	General Hospital	Class 2	880.5440	2023-05-22
EHL	Point, Abrasive	Dental	Class 1	872.6010	2012-07-09

Official Correspondent

Mary Tsai

US Agent Details

Meng T. Tan Email: mengtan@msn.com Phone: (626) 2023457

Related Public Records

Same Entity

CHI FENG CO.,LTD

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
K243985	Icu Medical, Inc.	Rio Drug Reconstitution Transfer Device	2025-01-22
K222718	Hangzhou Qiantang Longyue Biotechnology Co., Ltd.	Vial Adapter	2023-03-10

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0007-2017	Baxter Corporation Englewood	2	0.2 Micron Filter, 50 mm Product Usage: The 0.2 Micron Filter is a bacteria and particulate filter for aqueous solutions. It attaches to a standard Baxter Pharmacy Pump Tube Set.

Similar Registrations

Registration Number	Establishment Name	Location
3015259866	SWIK Medical Solutions	Farmington Hills, MI, US
3013584824	ERGOMEDI LTD.	Espoo Uusimaa, FI
3015703934	MEDFRUITION ELECTRONICS TECHNOLOGY CO., LTD	Foshan City Guangdong, CN
3038718579	OKETZ LOGISTICS LLC	Coral Gables, FL, US
3010162973	Synergy Health Marseille SAS	MARSEILLE CEDEX 14 Provence-Alpes-Cote d'Azur, FR

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3006979803. Last updated year: 2026. Please use registration number 3006979803 when referencing this establishment in official correspondence.