Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3020294761

FEI Number

3020294761

Entity Name

ZHEJIANG CHIMIN TANG MEDICINE TRADE CO., LTD.

City/State/Country

Taizhou Zhejiang, CN

Establishment Address

888 Beiyuan Road, Huangyan, Taizhou Zhejiang 318020, CN

Establishment Type(s)

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

Owner / Operator

Zhejiang Chimin Tang Medicine Trade Co., Ltd. (Owner Number: 10082349)

Owner / Operator Contact Address

888 Beiyuan Road, Huangyan, Taizhou, CN-ZJ 318020, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K980069

PMA Number

N/A

All Registered Proprietary Names

Vanishpoint Easypoint Vanishpoint Vanishpoint Vanishpoint

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
MEG	Syringe, Antistick	General Hospital	Class 2	880.5860	2021-07-14
FMI	Needle, Hypodermic, Single Lumen	General Hospital	Class 2	880.5570	2021-07-14
MEG	Syringe, Antistick	General Hospital	Class 2	880.5860	2021-07-14
MEG	Syringe, Antistick	General Hospital	Class 2	880.5860	2021-07-14
MEG	Syringe, Antistick	General Hospital	Class 2	880.5860	2021-07-14

Official Correspondent

Yang Yang

US Agent Details

Michele Larios Business: Retractable Technologies Inc Email: rtilegal@retractable.com Phone: (972) 2941010

Related Public Records

Same Entity

Zhejiang Chimin Tang Medicine Trade 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
K092413	Inviro Medical Devices, Inc.	INVIROSNAP 50 AND 100 UNIT INSULIN SAFETY SYRINGES	2009-09-04
K163162	Jiangxi Hongda Medical Equipment Group , Ltd.	Sterile Hypodermic Safety Syringes for Single Use	2017-03-20
K812404	Nu Tech Medical Systems	BUTTERFLY NEEDLE ASSEMBLY	1981-09-09

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0002-2022	Bard Peripheral Vascular Inc	2	REF TIN3015, 15G x 79 mm Bone Marrow Aspiration/Intraosseous Infusion Needle, For Single Use Only, Sterile EO, UDI: 10885403043796

Similar Registrations

Registration Number	Establishment Name	Location
3027338968	RONCADELLE OPERATIONS SRL	Castel Mella Brescia, IT
3029328631	PEGASUS IMPORTS	Houston, TX, US
3012116434	ANHUI HONGYU WUZHOU MEDICAL MANUFACTURER CO., LTD.	Taihu Anhui, CN
3015528193	Almac Pharma Services (Ireland) Limited	Dundalk Louth, IE
3008719222	ZHEJIANG LONGDE PHARMACEUTICAL Co., Ltd	HANGZHOU Zhejiang, CN

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3020294761. Last updated year: 2026. Please use registration number 3020294761 when referencing this establishment in official correspondence.