Taiwan FDA registration b0dae13f530b7c743e2466437a134faf

“Asclepion” MultiPulse Ho Laser System

TW: “亞斯克雷皮恩”多波光鈥雷射系統
Taiwan flagTaiwan·Risk Class 2·MD·Asclepion Laser Technologies GmbH·Registered Jun 23, 2021 – Jun 23, 2026Expired
Registration details
Analysis ID
b0dae13f530b7c743e2466437a134faf
License Form
Ministry of Health Medical Device Import No. 034682
Customs Code
DHA05603468204
Company information
Manufacturer Country
Germany
Authorized Representative
JIANHE BIO-MEDICAL LTD.
Product details
Intended Use
Details are as detailed as approved Chinese instructions
Product Type (Level 1)
I General and plastic surgical devices
Product Type (Level 2)
I4810 Lasers for general surgery, plastic surgery and dermatology
Import Information
Imported from abroad
Dates and status
Registration Date
Jun 23, 2021
Expiry Date
Jun 23, 2026
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About this record

Access comprehensive regulatory information for “Asclepion” MultiPulse Ho 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 b0dae13f530b7c743e2466437a134faf and manufactured by Asclepion Laser Technologies GmbH. The authorized representative in Taiwan is JIANHE BIO-MEDICAL LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including ASCLEPION LASER TECHNOLOGIES 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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