Taiwan FDA registration 5dc8e472a6ee2b73cf4d2a3155a6a896

"DORNIER" Medilor diode laser

TW: “多尼爾”美帝樂二極體雷射
Taiwan flagTaiwan·Risk Class 2·DORNIER MEDTECH GMBH; Dornier MedTech Laser GmbH·Registered Sep 21, 2012 – Sep 21, 2017Cancelled
Registration details
Analysis ID
5dc8e472a6ee2b73cf4d2a3155a6a896
Customs Code
DHA00602403804
Company information
Manufacturer Country
Germany
Authorized Representative
VICTORY EIGHT ENTERPRISE CO., LTD.
Product details
Intended Use
For details, it is Chinese approved copy of the imitation order
Product Type (Level 1)
I General, Plastic Surgery and Dermatology
Product Type (Level 2)
I.4810 Lasers for general surgical, orthopaedic and dermatological use
Import Information
import
Dates and status
Registration Date
Sep 21, 2012
Expiry Date
Sep 21, 2017
Cancellation Date
Dec 13, 2019
Cancellation information
Status
Logged out
Reason
許可證已逾有效期
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About this record

Access comprehensive regulatory information for "DORNIER" Medilor diode laser in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 5dc8e472a6ee2b73cf4d2a3155a6a896 and manufactured by DORNIER MEDTECH GMBH; Dornier MedTech Laser GmbH. The authorized representative in Taiwan is VICTORY EIGHT ENTERPRISE CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including DORNIER MEDTECH GMBH; Dornier MedTech Laser GmbH, and 3 recent registrations in the same category. 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.

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