Globalcare Medical Technology HK, Ltd.

FDA Device Registration & Listing · Hong Kong, HK · Registration 3010205626

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
3010205626
FEI Number
3010205626
Entity Name
Globalcare Medical Technology HK, Ltd.
City/State/Country
Hong Kong, HK
Establishment Address
Room25 4/F, Tung Hip Commercial Building 244 Des Voeux Rd Central, Sheung Wan, Hong Kong, Hong Kong NA, HK
Establishment Type(s)
Export Device to the United States But Perform No Other Operation on Device
Owner / Operator
Globalcare Medical Technology HK, Ltd. (Owner Number: 10046453)
Owner / Operator Contact Address
Room25 4/F, Tung Hip Commercial Building 244 Des Voeux Rd Central, Sheung Wan, Hong Kong, Hong Kong, HK-NOTA 999077, HK
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
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
HGX Pump, Breast, Powered Obstetrics/Gynecology Class 2 884.5160 2018-10-31
BYG Mask, Oxygen Anesthesiology Class 1 868.5580 2020-10-18
CAF Nebulizer (Direct Patient Interface) Anesthesiology Class 2 868.5630 2014-03-24
CAF Nebulizer (Direct Patient Interface) Anesthesiology Class 2 868.5630 2014-03-24
OCR Lung Sound Monitor Cardiovascular Class 2 870.1875 2023-06-14
CAF Nebulizer (Direct Patient Interface) Anesthesiology Class 2 868.5630 2020-09-02

Official Correspondent

Cherry Feng

US Agent Details

Terrence O'Brien Business: Project Marketing Email: 1968sfp@gmail.com Phone: (919) 6231053

Related Public Records

Same Entity

Globalcare Medical Technology HK, 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
K190465 Hygeia II Medical Group, Inc. Evolve Breast Pump 2019-10-18
K021739 Limerick, Inc. LIMERICK POWERED ELECTRIC BREAST PUMP MODEL 1002 2003-01-10
K163485 Adherium (Nz), Ltd. SmartTouch 2017-08-30
K781467 Travenol Laboratories, S.A. U-FLOAT VALVE 2D9023 1978-09-07

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3010205626. Last updated year: 2026. Please use registration number 3010205626 when referencing this establishment in official correspondence.
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