Taiwan FDA registration 1c2ed33bfc50a02da3c3c5d66d80868e

"Fan Mei" hyperbaric oxygen therapy chamber

TW: “範美”高壓氧治療艙
Taiwan flagTaiwan·Risk Class 2·Fanmei High Oxygen Biomedical Technology Co., Ltd. Kaohsiung Factory·Registered Dec 05, 2011 – Dec 05, 2026Active
Registration details
Analysis ID
1c2ed33bfc50a02da3c3c5d66d80868e
Customs Code
DHY00500344002
Company information
Manufacturer Country
Taiwan, Province of China
Product details
Intended Use
For details, it is Chinese approved copy of the imitation order
Product Type (Level 1)
D Anesthesiology
Product Type (Level 2)
D.5470 Hyperbaric chamber
Import Information
Domestic;; 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
Registration Date
Dec 05, 2011
Expiry Date
Dec 05, 2026
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About this record

Access comprehensive regulatory information for "Fan Mei" hyperbaric oxygen therapy chamber in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 1c2ed33bfc50a02da3c3c5d66d80868e and manufactured by Fanmei High Oxygen Biomedical Technology Co., Ltd. Kaohsiung Factory. The authorized representative in Taiwan is Fanmei High Oxygen Biomedical Technology Co., Ltd.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Fanmei High Oxygen Biomedical Technology Co., Ltd. Kaohsiung Factory, and 1 recent registrations in the same category. 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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