Taiwan FDA registration 8d3a2b03ebc4405e7a076abcd220555f

"Jielu" vacuum collection bottle (unsterilized)

TW: “捷銳”真空收集瓶 (未滅菌)

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

Registration details

Analysis ID: 8d3a2b03ebc4405e7a076abcd220555f
Customs Code: DHA04600047708

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: Input;; Chinese goods;; QMS/QSD

Dates and status

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

About this record

Access comprehensive regulatory information for "Jielu" vacuum collection bottle (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 8d3a2b03ebc4405e7a076abcd220555f and manufactured by GENTEC (SHANGHAI) CORPORATION. The authorized representative in Taiwan is COLUMBIA EQUIPMENT CORPORATION.

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