Taiwan FDA registration 416093aaf826e5fb1a28f218ff7f8f38
"Fresenius Kabi" Knoss sensor
TW: “費森尤斯卡比”克諾斯感應器
Registration details
- Analysis ID
- 416093aaf826e5fb1a28f218ff7f8f38
- Customs Code
- DHA09200111709
Company information
- Manufacturer Country
- Spain;;China
- Authorized Representative
- FRESENIUS KABI TAIWAN LIMITED
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- K Neuroscience
- Product Type (Level 2)
- K.1320 Skin electrode
- Import Information
- Contract manufacturing;; Input;; Chinese goods
Dates and status
- Registration Date
- Mar 05, 2020
- Expiry Date
- Mar 05, 2025
About this record
Access comprehensive regulatory information for "Fresenius Kabi" Knoss sensor in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 416093aaf826e5fb1a28f218ff7f8f38 and manufactured by Quantium Medical S.L.U;; Shenzhen Med-Link Electronics Tech Co., Ltd. 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 DatabasePowered by Pure Global AI89,000+ Devices