Asia Automax

FDA Device Registration & Listing · Qingpu District Shanghai, CN · Registration 3012236175

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
3012236175
FEI Number
3012236175
Entity Name
Asia Automax
City/State/Country
Qingpu District Shanghai, CN
Establishment Address
Building 1, No. 2400, Huqingping Rd, Xujin Town, Qingpu District Shanghai 201702, CN
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Asia Automax Shanghai (Owner Number: 10079525)
Owner / Operator Contact Address
Building 1, No. 2400, Huqingping Rd,, Xujin Town, Qingpu District, CN-SH 201702, CN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Tommie Copper

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
FQL Stocking, Medical Support (For General Medical Purposes) General Hospital Class 1 880.5780 2020-12-10
FQM Bandage, Elastic General Hospital Class 1 880.5075 2024-01-11

Official Correspondent

Jane Lu

US Agent Details

Lauren Chiacchia Business: Tommie Copper Inc Email: Lauren@tommiecopper.com Phone: (914) 2156427

Related Public Records

Same Entity

Asia Automax Shanghai
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3012236175. Last updated year: 2026. Please use registration number 3012236175 when referencing this establishment in official correspondence.
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