Taiwan FDA registration 196e7347edea36c08e348198bd53fa89
AVOXimeter 1000E Whole Blood Oximeter
TW: 艾佛克斯血氧飽和測定儀
Registration details
- Analysis ID
- 196e7347edea36c08e348198bd53fa89
- License Form
- Ministry of Health Medical Device Import No. 026228
- Customs Code
- DHA05602622802
Company information
- Manufacturer
- Accriva Diagnostics Inc.
- Manufacturer Country
- United States
- Authorized Representative
- Werfen Taiwan Limited
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- E Cardiovascular devices
- Product Type (Level 2)
- E2700 Oximeter
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jun 05, 2014
- Expiry Date
- Jun 05, 2024
About this record
Access comprehensive regulatory information for AVOXimeter 1000E Whole Blood Oximeter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 196e7347edea36c08e348198bd53fa89 and manufactured by Accriva Diagnostics Inc.. The authorized representative in Taiwan is Werfen 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.
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