Taiwan FDA registration ce716cb4a4d5bebea85e11844f1e2b83

"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 Dec 19, 2007 – Dec 19, 2017Cancelled
Registration details
Analysis ID
ce716cb4a4d5bebea85e11844f1e2b83
Customs Code
DHA00601850701
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
Dec 19, 2007
Expiry Date
Dec 19, 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 ce716cb4a4d5bebea85e11844f1e2b83 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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