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“PENTAX MEDICAL” VIDEO NASO-PHARYNGO-LARYNGOSCOPE - Taiwan Registration c58b89538c8551cc3e676fc6ac2a4cde

Access comprehensive regulatory information for “PENTAX MEDICAL” VIDEO NASO-PHARYNGO-LARYNGOSCOPE in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c58b89538c8551cc3e676fc6ac2a4cde and manufactured by HOYA CORPORATION PENTAX MIYAGI FACTORY. The authorized representative in Taiwan is PENTAX MEDICAL SINGAPORE PTE. LTD. TAIWAN BRANCH(SINGAPORE).

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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c58b89538c8551cc3e676fc6ac2a4cde
Registration Details
Taiwan FDA Registration: c58b89538c8551cc3e676fc6ac2a4cde
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Device Details

“PENTAX MEDICAL” VIDEO NASO-PHARYNGO-LARYNGOSCOPE
TW: “賓得醫療”電子式鼻咽喉內視鏡
Risk Class 2
MD

Registration Details

c58b89538c8551cc3e676fc6ac2a4cde

Ministry of Health Medical Device Import No. 029643

DHA05602964300

Product Details

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

G ENT device

G4760 Nasopharyngeal scope (soft or rigid) and its accessories

Imported from abroad

Dates and Status

Apr 21, 2017

Apr 21, 2027