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"MAXER" Laryngostroboscope (Non-Sterile) - Taiwan Registration 481e07af71208eb2e6a40c2a9dfaccae

Access comprehensive regulatory information for "MAXER" 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 481e07af71208eb2e6a40c2a9dfaccae and manufactured by MAXER MEDIZINTECHNIK GMBH. The authorized representative in Taiwan is HIGH TOP MEDICAL CO., LTD..

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481e07af71208eb2e6a40c2a9dfaccae
Registration Details
Taiwan FDA Registration: 481e07af71208eb2e6a40c2a9dfaccae
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Device Details

"MAXER" Laryngostroboscope (Non-Sterile)
TW: "้บฅๅ…‹ๆ–ฏ็ˆพ" ๅ–‰้ ญ้–ƒ้ ปๅ…ง่ฆ–้ก (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

481e07af71208eb2e6a40c2a9dfaccae

Ministry of Health Medical Device Import No. 019893

DHA09401989301

Company Information

Germany

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

Dec 06, 2018

Dec 06, 2023