Taiwan FDA registration fa370e1be561bd389e44af1bca6a9dbb
"Reis" aspiration aid (unsterilized)
TW: “瑞斯”吸藥輔助器 (未滅菌)
Taiwan·Risk Class 1·RESPIRONICS, INC.·Registered Jun 23, 2006 – Jun 23, 2011CancelledRegistration details
- Analysis ID
- fa370e1be561bd389e44af1bca6a9dbb
- Customs Code
- DHA04400478408
Company information
- Manufacturer
- RESPIRONICS, INC.
- Manufacturer Country
- United States
- Authorized Representative
- BIOSYSTEMS INC.
Product details
- Intended Use
- Limited to the scope of the first class of the medical equipment management method "Non-respiratory medical aerosol (D.5640)".
- Product Type (Level 1)
- D Anesthesiology
- Product Type (Level 2)
- D.5640 非呼吸用醫藥噴霧器(atomizer)
- Import Information
- import
Dates and status
- Registration Date
- Jun 23, 2006
- Expiry Date
- Jun 23, 2011
- Cancellation Date
- Nov 22, 2012
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Reis" aspiration aid (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number fa370e1be561bd389e44af1bca6a9dbb and manufactured by RESPIRONICS, INC.. The authorized representative in Taiwan is BIOSYSTEMS INC..
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