Taiwan FDA registration 16a464fc04b0a237361d25c3936acad7
"Vyaire” Bacterial/viral Filter kits
TW: “維亞爾＂細菌過濾器組
Taiwan·Risk Class 2·MD·Vyaire Medical GmbH·Registered Mar 25, 2014 – Mar 25, 2024ExpiredRegistration details
- Analysis ID
- 16a464fc04b0a237361d25c3936acad7
- License Form
- Ministry of Health Medical Device Import No. 026022
- Customs Code
- DHA05602602205
Company information
- Manufacturer
- Vyaire Medical GmbH
- Manufacturer Country
- Germany
- Authorized Representative
- BIOSYSTEMS INC.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- D Devices for anesthesiology
- Product Type (Level 2)
- D5260 Breathing line bacterial filter
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Mar 25, 2014
- Expiry Date
- Mar 25, 2024
About this record
Access comprehensive regulatory information for "Vyaire” Bacterial/viral Filter kits in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 16a464fc04b0a237361d25c3936acad7 and manufactured by Vyaire Medical GmbH. The authorized representative in Taiwan is BIOSYSTEMS INC..
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