Taiwan FDA registration fd7338d99c07e6efd83555937026f609
"Priglai" eye laser probe
TW: “普瑞格萊”眼用雷射探針
Taiwan·Risk Class 2·Peregrine Surgical Ltd.·Registered Apr 23, 2013 – Apr 23, 2028ActiveRegistration details
- Analysis ID
- fd7338d99c07e6efd83555937026f609
- Customs Code
- DHA00602459500
Company information
- Manufacturer
- Peregrine Surgical Ltd.
- Manufacturer Country
- United States
- Authorized Representative
- (Hong Kong) Lumenis Be (HK) Limited, Taiwan Branch
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- M Ophthalmology
- Product Type (Level 2)
- M.4390 眼科雷射裝置
- Import Information
- import
Dates and status
- Registration Date
- Apr 23, 2013
- Expiry Date
- Apr 23, 2028
About this record
Access comprehensive regulatory information for "Priglai" eye laser probe in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number fd7338d99c07e6efd83555937026f609 and manufactured by Peregrine Surgical Ltd.. The authorized representative in Taiwan is (Hong Kong) Lumenis Be (HK) Limited, Taiwan Branch.
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