Taiwan FDA registration cdb98ef10f5c68d9b0bae07875ad9a8c
VenAir Sequential Compression System
TW: “雃博”連續加壓系統
Taiwan·Risk Class 2·MD·Wellell Inc.·Registered Apr 20, 2022 – Apr 20, 2027ActiveRegistration details
- Analysis ID
- cdb98ef10f5c68d9b0bae07875ad9a8c
- License Form
- Ministry of Health Medical Device Manufacturing No. 007457
Company information
- Manufacturer
- Wellell Inc.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- Wellell Inc.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Product Type (Level 2)
- E5800 Compression sleeve for extremities
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Apr 20, 2022
- Expiry Date
- Apr 20, 2027
About this record
Access comprehensive regulatory information for VenAir Sequential Compression System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number cdb98ef10f5c68d9b0bae07875ad9a8c and manufactured by Wellell Inc.. The authorized representative in Taiwan is Wellell Inc..
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