"Mizushibi" respirator
- Analysis ID
- 976b2c24914311f5d4735774a47d265d
- Customs Code
- DHA00601274401
- Manufacturer
- RESMED LIMITED
- Manufacturer Country
- Australia
- Authorized Representative
- BROJAW INC.
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- D Anesthesiology
- Product Type (Level 2)
- D.5905 Non-continuous respirators
- Import Information
- import
- Registration Date
- Oct 20, 2005
- Expiry Date
- Oct 20, 2015
- Cancellation Date
- May 17, 2018
- Status
- Logged out
- Reason
- 許可證已逾有效期
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Access comprehensive regulatory information for "Mizushibi" respirator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 976b2c24914311f5d4735774a47d265d and manufactured by RESMED LIMITED. The authorized representative in Taiwan is BROJAW INC..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including RESMED LTD., and 1 recent registrations in the same category. 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.