Taiwan FDA registration 9b2270bb715b2b4c9288f4678f864e83
Dar medical sieve atomizer and its accessories
TW: 達爾醫用篩孔式霧化器及其配件
Registration details
- Analysis ID
- 9b2270bb715b2b4c9288f4678f864e83
- Customs Code
- DHA09200080805
Company information
- Manufacturer
- DELBIO (WUJIANG) CO., LTD.
- Manufacturer Country
- China
- Authorized Representative
- DELBIO INC.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- D Anesthesiology
- Product Type (Level 2)
- D.5630 Nebulizer
- Import Information
- Chinese goods;; input
Dates and status
- Registration Date
- Dec 27, 2016
- Expiry Date
- Dec 27, 2026
About this record
Access comprehensive regulatory information for Dar medical sieve atomizer and its accessories in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 9b2270bb715b2b4c9288f4678f864e83 and manufactured by DELBIO (WUJIANG) CO., LTD.. The authorized representative in Taiwan is DELBIO 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.
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