Taiwan FDA registration 9e34596603017a47f19de06e5c5b9ca0

"SK MEDITECH" X-Ray Protective Device (Non-Sterile)

TW: "舒況麥迪泰克" X光防護用具 (未滅菌)

Taiwan·Risk Class 1·MD·SK MEDITECH. CO., LTD.·Registered Jan 08, 2021 – Jan 08, 2026Expired

Registration details

Analysis ID: 9e34596603017a47f19de06e5c5b9ca0
License Form: Ministry of Health Medical Device Import No. 022236
Customs Code: DHA09402223601

Company information

Manufacturer: SK MEDITECH. CO., LTD.
Manufacturer Country: Korea, Republic of
Authorized Representative: Shiang Tai Medical Instructment CO., LTD.

Product details

Intended Use: Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Personal Protective Shield (P.6500)".
Product Type (Level 1): P Devices for radiology
Product Type (Level 2): P6500 Personal Shield
Import Information: Imported from abroad

Dates and status

Registration Date: Jan 08, 2021
Expiry Date: Jan 08, 2026

About this record

Access comprehensive regulatory information for "SK MEDITECH" X-Ray Protective Device (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 9e34596603017a47f19de06e5c5b9ca0 and manufactured by SK MEDITECH. CO., LTD.. The authorized representative in Taiwan is Shiang Tai Medical Instructment CO., LTD..

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