Taiwan FDA registration 2979de80a8bc2a17b86dbba6b5baa79c

"Lisa" Reflex laser system

TW: "麗沙"瑞福雷斯雷射系統
Taiwan flagTaiwan·Risk Class 2·LISA Laser Products GmbH·Registered Dec 11, 2006 – Dec 11, 2021Cancelled
Registration details
Analysis ID
2979de80a8bc2a17b86dbba6b5baa79c
Customs Code
DHA00601747802
Company information
Manufacturer Country
Germany
Authorized Representative
REVO LASER CORPORATION
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 11, 2006
Expiry Date
Dec 11, 2021
Cancellation Date
Aug 15, 2023
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 "Lisa" Reflex laser system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2979de80a8bc2a17b86dbba6b5baa79c and manufactured by LISA Laser Products GmbH. The authorized representative in Taiwan is REVO LASER CORPORATION.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including LISA Laser Products GmbH, and 1 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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