FDA Registration Active 🇨🇳 China

GUANGZHOU IMPROVE MEDICAL INSTRUMENTS CO., LTD.

Reg #: 3008449424 · FEI: 3008449424 · Expires 2026
Products
6
Proprietary Names
16
Establishment Types
3
Classifications
6

Registration Details

Registration Name
GUANGZHOU IMPROVE MEDICAL INSTRUMENTS CO., LTD.
Registration Number
3008449424
FEI Number
3008449424
Status
Active
Expiry Year
2026
Initial Importer
No
Address
No.102, Kaiyuan Avenue, Science City, Guangzhou Economic & Technological Development District
City
Guangzhou Guangdong
Country
CN

Regulatory Submissions

510(k) Number
K153388

Owner / Operator

Firm Name
Guangzhou Improve Medical Instruments Co., Ltd.
Operator Number
10038705
Address
No.102, Kaiyuan Avenue, Science City, Guangzhou Economic & Technological Development District, PEOPLE'S REPUBLIC OF CHINA
City
Guangzhou
State
Guangdong
Postal Code
510530
Country
CN

US Agent

Business Name
IMPROVE MEDICAL USA, INC.
Contact Name
Chang Che
Address
2195 Faraday Ave Ste B
City
Carlsbad
State
CA
ZIP
92008
Country
US
Phone
760 2018878

Products

Device Name Product Code
Needle, Hypodermic, Single Lumen FMI
Tubes, Vials, Systems, Serum Separators, Blood Collection JKA
Tourniquet, Nonpneumatic GAX
Container, Specimen, Sterile FMH
System, Blood Collection, Vacuum-Assisted, Manual KST
Container, Specimen, Non-Sterile NNI

Proprietary Names

IMPROVACUTER® Multi Sample Needle IMPROSAFE® Multi Sample Needle (Flashback) IMPROVACUTER® Blood Collection Set Pre-attached Holder IMPROSAFE® Blood Collection Set with Pre-attached Holder IMPROSAFE® Multi Sample Needle IMPROSAFE® Blood Collection Set IMPROVACUTER® Blood Collection Set Improve Blood Collection Set and Improsafe Blood Collection Set TOURNIQUET, NONPNEUMATIC Urinalysis No Additive Tube No Additive Tube Urinalysis Preservative Tube No Additive (Z) Tube IMPROVACUTER® Gel & Clot Activator Tube Needle Holder Urine Collection Container

Establishment Types

Manufacture Medical Device Manufacture Medical Device for Another Party (Contract Manufacturer) Develop Specifications But Do Not Manufacture At This Facility