Taiwan FDA registration cbfe369b39d20391c6c237524a3880d7
"Kaile" otoscopy (unsterilized)
TW: "凱樂"耳鏡(未滅菌)
Taiwan·Risk Class 1·KEELER LTD.·Registered Apr 11, 2006 – Apr 11, 2026ExpiredRegistration details
- Analysis ID
- cbfe369b39d20391c6c237524a3880d7
- Customs Code
- DHA04400359207
Company information
- Manufacturer
- KEELER LTD.
- Manufacturer Country
- United Kingdom
- Authorized Representative
- TAIWAN OPTICAL CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of the "Otoscope (G.4770)" of the Administrative Measures for the Classification and Grading of Medical Equipment.
- Product Type (Level 1)
- G ENT Science
- Product Type (Level 2)
- G.4770 Ear Mirrors
- Import Information
- import
Dates and status
- Registration Date
- Apr 11, 2006
- Expiry Date
- Apr 11, 2026
About this record
Access comprehensive regulatory information for "Kaile" otoscopy (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number cbfe369b39d20391c6c237524a3880d7 and manufactured by KEELER LTD.. The authorized representative in Taiwan is TAIWAN OPTICAL CO., LTD..
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