Taiwan FDA registration c3d92cd969fb6fc46113f7c65ca6dd0b

"Denmark" Qili pulsed light therapy instrument

TW: "丹麥" 綺麗脈衝光療儀
Taiwan flagTaiwan·DANISH DERMATOLOGIC DEVELOPMENT A/S·Registered Dec 30, 2003 – Dec 30, 2008Cancelled
Registration details
Analysis ID
c3d92cd969fb6fc46113f7c65ca6dd0b
Customs Code
DHA00601050407
Company information
Manufacturer Country
Denmark
Authorized Representative
FOCUSWAVE TECHNOLOGY CORPORATION
Product details
Intended Use
適用於:1.色素沉著病變 (PIGMENTED LESIONS),2.血管性病變(VASCULAR LESIONS):臉部微血管增生(FACIAL TELANGIECTASIAS),腿部微血管增生(LEG TELANGIECTASIAS),葡萄酒色斑(PORT-WINE STAINS). 3.除毛(HAIR REMOVAL).
Product Type (Level 1)
I General, Plastic Surgery and Dermatology
Import Information
import
Dates and status
Registration Date
Dec 30, 2003
Expiry Date
Dec 30, 2008
Cancellation Date
Apr 30, 2014
Cancellation information
Status
Logged out
Reason
許可證已逾有效期
About this record

Access comprehensive regulatory information for "Denmark" Qili pulsed light therapy instrument in Taiwan's medical device market through Pure Global AI's free database. is registered under number c3d92cd969fb6fc46113f7c65ca6dd0b and manufactured by DANISH DERMATOLOGIC DEVELOPMENT A/S. The authorized representative in Taiwan is FOCUSWAVE TECHNOLOGY CORPORATION.

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

Free DatabasePowered by Pure Global AI89,000+ Devices