Guilin Refine Medical Instrument Co L T D

FDA Filings

This page includes the latest FDA filings for Guilin Refine Medical Instrument Co L T D. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)
Registration Number3016075921
FEI Number3016075921
NameJames H Liao
Owner & OperatorGuilin Refine Medical Instrument Co., LTD.
Contact AddressNO.8-3, Information Industrial Park, Hig
Guilin CN-45 Guangxi 541004 CN
Official Correspondent
  • Judong Chen
  • 86-773-7790588-x
US Agent
Importing Logistics Registration
ImporterAPAX International, Inc.
Address6775 Verde Ridge Rd
Rancho Palos Verdes, CA 90275 UNITED STATES
Importer TypeBroker
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address6775 Verde Ridge Rd
Rancho Palos Verdes, CA 90275 US
Establishment TypeManufacture Medical Device



FDA Filings

Device
Company
DeviceDate
Guilin Refine Medical Instrument Co.,LTD.
REFINE 2023-12-14
Guilin Refine Medical Instrument Co.,LTD.
REFINE 2023-12-14
Guilin Refine Medical Instrument Co.,LTD.
REFINE 2023-12-14
Guilin Refine Medical Instrument Co.,LTD.
REFINE 2023-12-14
Guilin Refine Medical Instrument Co.,LTD.
REFINE 2023-12-05
Guilin Refine Medical Instrument Co.,LTD.
REFINE 2023-12-05
Guilin Refine Medical Instrument Co.,LTD.
REFINE 2023-12-05
Guilin Refine Medical Instrument Co.,LTD.
REFINE 2023-12-05
Guilin Refine Medical Instrument Co.,LTD.
REFINE 2023-12-05
Guilin Refine Medical Instrument Co.,LTD.
REFINE 2023-11-30
Guilin Refine Medical Instrument Co.,LTD.
REFINE 2022-09-30
Guilin Refine Medical Instrument Co.,LTD.
REFINE 2022-09-30
Guilin Refine Medical Instrument Co.,LTD.
REFINE 2022-09-30
Guilin Refine Medical Instrument Co.,LTD.
REFINE 2022-09-30
James H Liao [Guilin Refine Medical Instrument Co., LTD.]
Safety Goggle2020-03-26
James H Liao [Guilin Refine Medical Instrument Co., LTD.]
Face Shield2020-03-26

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