Taiwan FDA registration 279f7e13a6790fd7e831c06e03e22980

"Vanadium" Patient Examination Powder-free Gloves (Unsterilized)

TW: "釩泰"病患檢查用無粉手套(未滅菌)

Taiwan·Risk Class 1·BYTECH (DONGTAI) CO., LTD.·Registered May 24, 2018 – May 24, 2028Active

Registration details

Analysis ID: 279f7e13a6790fd7e831c06e03e22980
Customs Code: DHA09600343806

Company information

Manufacturer: BYTECH (DONGTAI) CO., LTD.
Manufacturer Country: China
Authorized Representative: FINETECH RESEARCH AND INNOVATION CORPORATION

Product details

Intended Use: Limited to the first level of identification scope of the Measures for the Classification and Grading of Medical Equipment "Gloves for Patient Examination (J.6250)".
Product Type (Level 1): J General hospital and personal use equipment
Product Type (Level 2): J.6250 病患檢查用手套
Import Information: QMS/QSD;; Input;; Chinese goods

Dates and status

Registration Date: May 24, 2018
Expiry Date: May 24, 2028

About this record

Access comprehensive regulatory information for "Vanadium" Patient Examination Powder-free Gloves (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 279f7e13a6790fd7e831c06e03e22980 and manufactured by BYTECH (DONGTAI) CO., LTD.. The authorized representative in Taiwan is FINETECH RESEARCH AND INNOVATION CORPORATION.

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