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“Asclepion” MultiPulse Ho Laser System - Taiwan Registration b0dae13f530b7c743e2466437a134faf

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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b0dae13f530b7c743e2466437a134faf
Registration Details
Taiwan FDA Registration: b0dae13f530b7c743e2466437a134faf
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Device Details

“Asclepion” MultiPulse Ho Laser System
TW: “亞斯克雷皮恩”多波光鈥雷射系統
Risk Class 2
MD

Registration Details

b0dae13f530b7c743e2466437a134faf

Ministry of Health Medical Device Import No. 034682

DHA05603468204

Company Information

Product Details

Details are as detailed as approved Chinese instructions

I General and plastic surgical devices

I4810 Lasers for general surgery, plastic surgery and dermatology

Imported from abroad

Dates and Status

Jun 23, 2021

Jun 23, 2026

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