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"Baitella" Ear, nose, and throat manual surgical instrument (Non-Sterile) - Taiwan Registration d9561030da8a0139610af17c8d1ee08b

Access comprehensive regulatory information for "Baitella" Ear, nose, and throat manual surgical instrument (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 d9561030da8a0139610af17c8d1ee08b and manufactured by BAITELLA AG. The authorized representative in Taiwan is FU TAI TRADING CO., LTD..

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d9561030da8a0139610af17c8d1ee08b
Registration Details
Taiwan FDA Registration: d9561030da8a0139610af17c8d1ee08b
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Device Details

"Baitella" Ear, nose, and throat manual surgical instrument (Non-Sterile)
TW: "่ฒๅพทๆ‹‰" ่€ณ้ผปๅ–‰ๆ‰‹ๅ‹•ๅผๅค–็ง‘ๅ™จๆขฐ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

d9561030da8a0139610af17c8d1ee08b

Ministry of Health Medical Device Import No. 016334

DHA09401633402

Company Information

Switzerland

Product Details

Limited to the first level identification scope of the Measures for the Administration of Medical Devices "ENT Manual Surgical Instruments (G.4420)".

G ENT device

G4420 OTOLARYNGARY Manual Surgical Instrument

Imported from abroad

Dates and Status

Mar 30, 2016

Mar 30, 2021