Pure Global

“HearMEC” AirForce Hyperbaric Oxygen Chamber O2 Prime Cabin - Taiwan Registration 6b6bcdd6bc9c01ff4b492e79b95d9bf6

Access comprehensive regulatory information for “HearMEC” AirForce Hyperbaric Oxygen Chamber O2 Prime Cabin in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 6b6bcdd6bc9c01ff4b492e79b95d9bf6 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.

Free Database
Powered by Pure Global AI
89,000+ Devices
6b6bcdd6bc9c01ff4b492e79b95d9bf6
Registration Details
Taiwan FDA Registration: 6b6bcdd6bc9c01ff4b492e79b95d9bf6
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

“HearMEC” AirForce Hyperbaric Oxygen Chamber O2 Prime Cabin
TW: “哈美克” 溫和高壓氧艙
Risk Class 2
MD

Registration Details

6b6bcdd6bc9c01ff4b492e79b95d9bf6

Ministry of Health Medical Device Import No. 035959

DHA05603595900

Company Information

Japan

Product Details

Details are as detailed as approved Chinese instructions

D Anesthesiology

D5470 Hyperbaric oxygen chamber

Imported from abroad

Dates and Status

Oct 10, 2022

Oct 10, 2027