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"PENTAX MEDICAL" Laryngostroboscope (Non-Sterile) - Taiwan Registration c2631e07e54e4fbf9c7f8562225ac271

Access comprehensive regulatory information for "PENTAX MEDICAL" Laryngostroboscope (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 c2631e07e54e4fbf9c7f8562225ac271 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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c2631e07e54e4fbf9c7f8562225ac271
Registration Details
Taiwan FDA Registration: c2631e07e54e4fbf9c7f8562225ac271
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Device Details

"PENTAX MEDICAL" Laryngostroboscope (Non-Sterile)
TW: "่ณ“ๅพ—้†ซ็™‚" ๅ–‰้ ญ้–ƒ้ ปๅ…ง่ฆ–้ก (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

c2631e07e54e4fbf9c7f8562225ac271

Ministry of Health Medical Device Import No. 017547

DHA09401754708

Company Information

Product Details

Limited to the first level identification range of the Measures for the Administration of Medical Devices "Laryngeal Flash Endoscopy (G.4750)".

G ENT device

G4750 Laryngeal flash endoscope

Imported from abroad

Dates and Status

Mar 02, 2017

Mar 02, 2027