Taiwan FDA registration 49212bdc56eff28791f892b30905fbe3

"BEAMATE" Light source and accessories (Non-Sterile)

TW: "彼美特" 光源及附件 (未滅菌)

Taiwan·Risk Class 1·MD·TAYA INTERNATIONAL CO., LTD.·Registered Apr 21, 2021 – Apr 21, 2026Expired

Registration details

Analysis ID: 49212bdc56eff28791f892b30905fbe3
License Form: Ministry of Health Medical Device Import No. 022507
Customs Code: DHA09402250703

Company information

Manufacturer: TAYA INTERNATIONAL CO., LTD.
Manufacturer Country: Japan
Authorized Representative: IN ORDER CO., LTD.

Product details

Intended Use: Limited to the first level identification scope of the Measures for the Administration of Medical Devices "ENT Fiber Optic Light Source and Vehicle (G.4350)".
Product Type (Level 1): G ENT device
Product Type (Level 2): G4350 ENT fiber optic light source and vehicle
Import Information: Imported from abroad

Dates and status

Registration Date: Apr 21, 2021
Expiry Date: Apr 21, 2026

About this record

Access comprehensive regulatory information for "BEAMATE" Light source and accessories (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 49212bdc56eff28791f892b30905fbe3 and manufactured by TAYA INTERNATIONAL CO., LTD.. The authorized representative in Taiwan is IN ORDER CO., LTD..

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