Taiwan FDA registration d9561030da8a0139610af17c8d1ee08b

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

TW: "貝德拉" 耳鼻喉手動式外科器械 (未滅菌)

Taiwan·Risk Class 1·MD·BAITELLA AG·Registered Mar 30, 2016 – Mar 30, 2021Expired

Registration details

Analysis ID: d9561030da8a0139610af17c8d1ee08b
License Form: Ministry of Health Medical Device Import No. 016334
Customs Code: DHA09401633402

Company information

Manufacturer: BAITELLA AG
Manufacturer Country: Switzerland
Authorized Representative: FU TAI TRADING CO., LTD.

Product details

Intended Use: Limited to the first level identification scope of the Measures for the Administration of Medical Devices "ENT Manual Surgical Instruments (G.4420)".
Product Type (Level 1): G ENT device
Product Type (Level 2): G4420 OTOLARYNGARY Manual Surgical Instrument
Import Information: Imported from abroad

Dates and status

Registration Date: Mar 30, 2016
Expiry Date: Mar 30, 2021

About this record

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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