Taiwan FDA registration 42fd966c2507c37369cf5d0f04472560
"DiaSys" BioMajesty Lipase DC FS (non-sterile)
TW: "黛而西斯" 百滿佳脂解酶試劑 (未滅菌)
Taiwan·Risk Class 1·MD·DIASYS DIAGNOSTIC SYSTEMS GMBH·Registered Dec 21, 2015 – Dec 21, 2020CancelledRegistration details
- Analysis ID
- 42fd966c2507c37369cf5d0f04472560
- License Form
- Ministry of Health Medical Device Import No. 016001
- Customs Code
- DHA09401600101
Company information
- Manufacturer
- DIASYS DIAGNOSTIC SYSTEMS GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- SYSMEX TAIWAN CO., LTD.
Product details
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A1465 Lipolytic enzyme test system
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Dec 21, 2015
- Expiry Date
- Dec 21, 2020
- Cancellation Date
- Jul 15, 2022
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "DiaSys" BioMajesty Lipase DC FS (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 42fd966c2507c37369cf5d0f04472560 and manufactured by DIASYS DIAGNOSTIC SYSTEMS GMBH. The authorized representative in Taiwan is SYSMEX TAIWAN CO., LTD..
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