Taiwan FDA registration c3a473881836a294228b8dfa57cbd005
Teleflex Infant Nasal Breathing Device Tubing and Accessories (Unsterilized)
TW: “泰利福”嬰兒鼻呼吸器管路及附件 (未滅菌)
Taiwan·Risk Class 1·TELEFLEX MEDICAL·Registered Nov 04, 2011 – Nov 04, 2021CancelledRegistration details
- Analysis ID
- c3a473881836a294228b8dfa57cbd005
- Customs Code
- DHA04401101504
Company information
- Manufacturer
- TELEFLEX MEDICAL
- Manufacturer Country
- Mexico
- Authorized Representative
- BENQ MEDICAL TECHNOLOGY CORPORATION
Product details
- Intended Use
- It is limited to the first level of identification of the medical device management measures "gas mask head strap (D.5560)" and "respirator tubing (D.5975)".
- Product Type (Level 1)
- D Anesthesiology
- Product Type (Level 2)
- D.5975 Respirator Tubing;; D.5560 Aerophyric mask head strap
- Import Information
- import
Dates and status
- Registration Date
- Nov 04, 2011
- Expiry Date
- Nov 04, 2021
- Cancellation Date
- May 21, 2018
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for Teleflex Infant Nasal Breathing Device Tubing and Accessories (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number c3a473881836a294228b8dfa57cbd005 and manufactured by TELEFLEX MEDICAL. The authorized representative in Taiwan is BENQ MEDICAL TECHNOLOGY CORPORATION.
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