Taiwan FDA registration ce36f17c6884db23b30ef5864e5c75d3
"Keeler" Operating Headlamp (Non-Sterile)
TW: "凱勒" 手術用頭燈 (未滅菌)
Taiwan·Risk Class 1·MD·Keeler Limited·Registered Apr 21, 2020 – Apr 21, 2025ExpiredRegistration details
- Analysis ID
- ce36f17c6884db23b30ef5864e5c75d3
- License Form
- Ministry of Health Medical Device Import No. 021479
- Customs Code
- DHA09402147906
Company information
- Manufacturer
- Keeler Limited
- Manufacturer Country
- United Kingdom
- Authorized Representative
- TAIWAN INSTRUMENT CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of the Measures for the Administration of Medical Devices "Surgical Headlamps (M.4335)".
- Product Type (Level 1)
- M Ophthalmic devices
- Product Type (Level 2)
- M4335 Surgical headlamp
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Apr 21, 2020
- Expiry Date
- Apr 21, 2025
About this record
Access comprehensive regulatory information for "Keeler" Operating Headlamp (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 ce36f17c6884db23b30ef5864e5c75d3 and manufactured by Keeler Limited. The authorized representative in Taiwan is TAIWAN INSTRUMENT CO., LTD..
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