Pure Global

"Kabi" Ambi-Implantable Injection System - Taiwan Registration 237090ec4422d2a934635232a3f7d7e2

Access comprehensive regulatory information for "Kabi" Ambi-Implantable Injection System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 237090ec4422d2a934635232a3f7d7e2 and manufactured by Fresenius Kabi AG;; CLINICO MEDICAL SP. Z.O.O. BลONIE NEAR WROCลAW. The authorized representative in Taiwan is FRESENIUS KABI TAIWAN LIMITED.

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.

Free Database
Powered by Pure Global AI
89,000+ Devices
237090ec4422d2a934635232a3f7d7e2
Registration Details
Taiwan FDA Registration: 237090ec4422d2a934635232a3f7d7e2
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Kabi" Ambi-Implantable Injection System
TW: โ€œๅกๆฏ”โ€ๅฎ‰ๆฏ”้ฉๆคๅ…ฅๅž‹ๆณจๅฐ„็ณป็ตฑ
Risk Class 2

Registration Details

237090ec4422d2a934635232a3f7d7e2

DHA05603035100

Company Information

Product Details

For details, it is Chinese approved copy of the imitation order

J General hospital and personal use equipment

J.5965 Subcutaneous implantable intravascular injection port and guide

import

Dates and Status

Oct 18, 2017

Oct 18, 2027