Taiwan FDA registration 5e0d125fbe8d0f8a62fc6626068a5668
"Teleflex" Medicinal Nonventilatory Nebulizer (Atomizer) (Non-sterile)
TW: "泰利福" 非呼吸用醫藥噴霧器 (未滅菌)
Taiwan·Risk Class 1·MD·TELEFLEX MEDICAL·Registered Nov 12, 2015 – Nov 12, 2020CancelledRegistration details
- Analysis ID
- 5e0d125fbe8d0f8a62fc6626068a5668
- License Form
- Ministry of Health Medical Device Import No. 015851
- Customs Code
- DHA09401585101
Company information
- Manufacturer
- TELEFLEX MEDICAL
- Manufacturer Country
- United States
- Authorized Representative
- BENQ MEDICAL TECHNOLOGY CORPORATION
Product details
- Product Type (Level 1)
- D Devices for anesthesiology
- Product Type (Level 2)
- D5640 Non-respiratory medical nebulizer
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Nov 12, 2015
- Expiry Date
- Nov 12, 2020
- Cancellation Date
- May 21, 2018
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for "Teleflex" Medicinal Nonventilatory Nebulizer (Atomizer) (Non-sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 5e0d125fbe8d0f8a62fc6626068a5668 and manufactured by TELEFLEX MEDICAL. The authorized representative in Taiwan is BENQ MEDICAL TECHNOLOGY CORPORATION.
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