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"Hamek" hyperbaric oxygen chamber - Taiwan Registration 2492a5f4710bc9b643ae9a08392e6e70

Access comprehensive regulatory information for "Hamek" hyperbaric oxygen chamber in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2492a5f4710bc9b643ae9a08392e6e70 and manufactured by HEARMEC CO., LTD.. The authorized representative in Taiwan is Health Way Biomedical Co., Ltd..

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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2492a5f4710bc9b643ae9a08392e6e70
Registration Details
Taiwan FDA Registration: 2492a5f4710bc9b643ae9a08392e6e70
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Device Details

"Hamek" hyperbaric oxygen chamber
TW: โ€œๅ“ˆ็พŽๅ…‹โ€้ซ˜ๅฃ“ๆฐง่‰™
Risk Class 2

Registration Details

2492a5f4710bc9b643ae9a08392e6e70

DHA05603377200

Company Information

Japan

Product Details

For details, it is Chinese approved copy of the imitation order

D Anesthesiology

D.5470 Hyperbaric chamber

Input;; The use of this device shall comply with the provisions of the Administrative Measures for the Implementation or Use of Medical Devices for Specific Medical Technology Inspection and Testing.

Dates and Status

Jun 19, 2020

Jun 19, 2025