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“PENTAX MEDICAL” VIDEO BRONCHOSCOPE - Taiwan Registration aacedc80267d397fb984101b65861ac0

Access comprehensive regulatory information for “PENTAX MEDICAL” VIDEO BRONCHOSCOPE in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number aacedc80267d397fb984101b65861ac0 and manufactured by HOYA CORPORATION PENTAX MIYAGI FACTORY. The authorized representative in Taiwan is PENTAX MEDICAL SINGAPORE PTE. LTD. TAIWAN BRANCH(SINGAPORE).

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aacedc80267d397fb984101b65861ac0
Registration Details
Taiwan FDA Registration: aacedc80267d397fb984101b65861ac0
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Device Details

“PENTAX MEDICAL” VIDEO BRONCHOSCOPE
TW: “賓得醫療”電子式支氣管鏡
Risk Class 2
MD

Registration Details

aacedc80267d397fb984101b65861ac0

Ministry of Health Medical Device Import No. 030319

DHA05603031904

Product Details

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

G ENT device

G4680 Bronchoscope (soft or rigid) and accessories

Imported from abroad

Dates and Status

Sep 30, 2017

Sep 30, 2027