Taiwan FDA registration cb855e7bec90f19fbd032ebc57625321
"Jessie" pulsed light system
TW: "婕曦"脈衝光系統
Taiwan·Risk Class 2·JEISYS MEDICAL INC.·Registered Aug 09, 2006 – Aug 09, 2016CancelledRegistration details
- Analysis ID
- cb855e7bec90f19fbd032ebc57625321
- Customs Code
- DHA00601697906
Company information
- Manufacturer
- JEISYS MEDICAL INC.
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- VICTORY EIGHT ENTERPRISE CO., LTD.
Product details
- Intended Use
- Hair removal, treatment / microvascular hyperplasia of the legs, port-wine pigmentation, pigmented lesions.
- Product Type (Level 1)
- P Radiology Science
- Product Type (Level 2)
- P.1750 電腦斷層掃描X光系統
- Import Information
- import
Dates and status
- Registration Date
- Aug 09, 2006
- Expiry Date
- Aug 09, 2016
- Cancellation Date
- May 28, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Jessie" pulsed light system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number cb855e7bec90f19fbd032ebc57625321 and manufactured by JEISYS MEDICAL INC.. The authorized representative in Taiwan is VICTORY EIGHT ENTERPRISE CO., LTD..
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