Taiwan FDA registration 71a6a5b29bfaf70d42bc8f13293b57f1
"KEELER" Transilluminator (Non-Sterile)
TW: "凱樂"透照器(未滅菌)
Taiwan·Risk Class 1·MD·KEELER LTD.·Registered Nov 21, 2013 – Nov 21, 2028ActiveRegistration details
- Analysis ID
- 71a6a5b29bfaf70d42bc8f13293b57f1
- License Form
- Ministry of Health Medical Device Import No. 013615
- Customs Code
- DHA09401361505
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 scope of the Measures for the Administration of Medical Devices "Translucent Apparatus (M.1945)".
- Product Type (Level 1)
- M Ophthalmic devices
- Product Type (Level 2)
- M1945 transillumination
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Nov 21, 2013
- Expiry Date
- Nov 21, 2028
About this record
Access comprehensive regulatory information for "KEELER" Transilluminator (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 71a6a5b29bfaf70d42bc8f13293b57f1 and manufactured by KEELER LTD.. The authorized representative in Taiwan is TAIWAN OPTICAL CO., LTD..
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