Taiwan FDA registration d39216e24328528d14fe04feb701fd9a
"Nakai hemp" ENT manual surgical instruments (unsterilized)
TW: “那蓋系麻”耳鼻喉手動式外科器械 (未滅菌)
Taiwan·Risk Class 1·NAGASHIMA MEDICAL INSTRUMENTS CO., LTD.·Registered Dec 19, 2013 – Dec 19, 2028ActiveRegistration details
- Analysis ID
- d39216e24328528d14fe04feb701fd9a
- Customs Code
- DHA09401369809
Company information
- Manufacturer
- NAGASHIMA MEDICAL INSTRUMENTS CO., LTD.
- Manufacturer Country
- Japan
- Authorized Representative
- WHOLE WELL CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of the classification and grading management method for medical equipment "ENT Manual Surgical Instruments (G.4420)".
- Product Type (Level 1)
- G ENT Science
- Product Type (Level 2)
- G.4420 Otolaryngology manual surgical instruments
- Import Information
- Input;; QMS/QSD
Dates and status
- Registration Date
- Dec 19, 2013
- Expiry Date
- Dec 19, 2028
About this record
Access comprehensive regulatory information for "Nakai hemp" ENT manual surgical instruments (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number d39216e24328528d14fe04feb701fd9a and manufactured by NAGASHIMA MEDICAL INSTRUMENTS CO., LTD.. The authorized representative in Taiwan is WHOLE WELL CO., LTD..
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