HANGZHOU SUPERDS INDUSTRY CO., LTD.

FDA Device Registration & Listing · Hangzhou City Zhejiang, CN · Registration 3010248787

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
3010248787
FEI Number
3010248787
Entity Name
HANGZHOU SUPERDS INDUSTRY CO., LTD.
City/State/Country
Hangzhou City Zhejiang, CN
Establishment Address
Taifeng Village, Zhongtai Township, Yuhang Dist, Hangzhou City Zhejiang 311121, CN
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
HANGZHOU SUPERDS INDUSTRY CO., LTD. (Owner Number: 10042997)
Owner / Operator Contact Address
Taifeng Village, Zhongtai Township, Yuhang Dist, Hangzhou City, CN-ZJ 311121, CN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

JODISMED TUBING, PRESSURE AND ACCESSORIES Oxygen Supply Tube Suction Connection Tube Oxygen Mask with Reservoir bag Venturi Mask Nasal Oxygen Cannula

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
BYX Tubing, Pressure And Accessories Anesthesiology Class 1 868.5860 2013-01-17
GAZ Tubing, Noninvasive General Hospital Class 2 880.6740 2013-01-17
KGB Mask, Oxygen, Non-Rebreathing Anesthesiology Class 1 868.5570 2013-01-17
BYF Mask, Oxygen, Low Concentration, Venturi Anesthesiology Class 1 868.5600 2013-01-17
CAT Cannula, Nasal, Oxygen Anesthesiology Class 1 868.5340 2013-01-17

Official Correspondent

FANG YAN

US Agent Details

Leeyeo Kee Business: Regrek LLC Email: regrek.cs@hotmail.com Phone: (302) 6089028

Related Public Records

Same Entity

HANGZHOU SUPERDS INDUSTRY 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
K910471 Baxter Healthcare Corp MEDID-VAC CLEAR NONCONDUCTIVE CONNECTING TUBE 1991-03-08

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3010248787. Last updated year: 2026. Please use registration number 3010248787 when referencing this establishment in official correspondence.
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