Taiwan FDA registration 9f2235af3835566afc2b5a815774ba21

Intesco endotracheal tube

TW: 茵特斯克氣管內管

Taiwan·Risk Class 2·JIANGSU WEIKANG JIEJING MEDICAL APPARATUS CO., LTD.;;INTERSURGICAL LTD·Registered Mar 19, 2018 – Mar 19, 2028Active

Registration details

Analysis ID: 9f2235af3835566afc2b5a815774ba21
Customs Code: DHA09200089207

Company information

Manufacturer: JIANGSU WEIKANG JIEJING MEDICAL APPARATUS CO., LTD.;;INTERSURGICAL LTD
Manufacturer Country: United Kingdom;;China
Authorized Representative: INTERSURGICAL TAIWAN LTD.

Product details

Intended Use: For details, it is Chinese approved copy of the imitation order
Product Type (Level 1): D Anesthesiology
Product Type (Level 2): D.5730 Endotracheal tubes
Import Information: Input;; Contract manufacturing;; Chinese goods

Dates and status

Registration Date: Mar 19, 2018
Expiry Date: Mar 19, 2028

About this record

Access comprehensive regulatory information for Intesco endotracheal tube in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 9f2235af3835566afc2b5a815774ba21 and manufactured by JIANGSU WEIKANG JIEJING MEDICAL APPARATUS CO., LTD.;;INTERSURGICAL LTD. The authorized representative in Taiwan is INTERSURGICAL TAIWAN LTD..

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.