Taiwan FDA registration 13a928e4a1af5f1f35390d0c066c58b2

"Jirui" vacuum suction regulator (unsterilized)

TW: “捷銳”真空抽吸調節器(未滅菌)

Taiwan·Risk Class 1·GENTEC (SHANGHAI) CORPORATION·Registered Jan 18, 2008 – Jan 18, 2028Active

Registration details

Analysis ID: 13a928e4a1af5f1f35390d0c066c58b2
Customs Code: DHA04600047504

Company information

Manufacturer: GENTEC (SHANGHAI) CORPORATION
Manufacturer Country: China
Authorized Representative: COLUMBIA EQUIPMENT CORPORATION

Product details

Intended Use: Limited to the first level recognition range of the classification and grading management measures for medical equipment "Vacuum-powered body fluid absorption device (J.6740)".
Product Type (Level 1): J General hospital and personal use equipment
Product Type (Level 2): J.6740 Vacuum-powered fluid absorption apparatus
Import Information: QMS/QSD;; Input;; Chinese goods

Dates and status

Registration Date: Jan 18, 2008
Expiry Date: Jan 18, 2028

About this record

Access comprehensive regulatory information for "Jirui" vacuum suction regulator (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 13a928e4a1af5f1f35390d0c066c58b2 and manufactured by GENTEC (SHANGHAI) CORPORATION. The authorized representative in Taiwan is COLUMBIA EQUIPMENT CORPORATION.

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