Taiwan FDA registration b4d4112edc26a4d8bc3ec4813e4a3800
"Camel Man" rigid laryngoscope (unsterilized)
TW: "駝人" 硬式喉頭鏡 (未滅菌)
Taiwan·Risk Class 1·HENAN TUOREN MEDICAL DEVICE CO., LTD.·Registered Jun 01, 2016 – Jun 01, 2021CancelledRegistration details
- Analysis ID
- b4d4112edc26a4d8bc3ec4813e4a3800
- Customs Code
- DHA09600273405
Company information
- Manufacturer
- HENAN TUOREN MEDICAL DEVICE CO., LTD.
- Manufacturer Country
- China
- Authorized Representative
- BIOTRONIC INSTRUMENT ENTERPRISE LTD.
Product details
- Intended Use
- Limited to the first level of identification scope of the Measures for the Administration of Medical Devices "Rigid Laryngoscopy (D.5540)".
- Product Type (Level 1)
- D Anesthesiology
- Product Type (Level 2)
- D.5540 Rigid laryngoscope
- Import Information
- Chinese goods;; input
Dates and status
- Registration Date
- Jun 01, 2016
- Expiry Date
- Jun 01, 2021
- Cancellation Date
- Sep 13, 2023
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Camel Man" rigid laryngoscope (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number b4d4112edc26a4d8bc3ec4813e4a3800 and manufactured by HENAN TUOREN MEDICAL DEVICE CO., LTD.. The authorized representative in Taiwan is BIOTRONIC INSTRUMENT ENTERPRISE LTD..
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