"PENTAX MEDICAL" Rebreathing device (Non-Sterile) - Taiwan Registration d5361aee317e8ff21313e2f17458063d
Access comprehensive regulatory information for "PENTAX MEDICAL" Rebreathing device (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number d5361aee317e8ff21313e2f17458063d and manufactured by PENTAX OF AMERICA, INC.. The authorized representative in Taiwan is PENTAX MEDICAL SINGAPORE PTE. LTD. TAIWAN BRANCH(SINGAPORE).
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Device Details
Registration Details
d5361aee317e8ff21313e2f17458063d
Ministry of Health Medical Device Import No. 017546
DHA09401754606
Product Details
Limited to the first level identification range of the Measures for the Administration of Medical Devices "Reinhalation Device (D.5675)".
D Devices for anesthesiology
D5675 Reinhalation device
Imported from abroad
Dates and Status
Mar 02, 2017
Mar 02, 2027