Taiwan FDA registration 3b4e9001a539b60f38dbc2f10098e773

"Asclepion" Manual surgical instrument for general use (Non-Sterile)

TW: "阿司克比恩" 一般手術用手動式器械 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·Asclepion Laser Technologies GmbH·Registered Oct 21, 2020 – Oct 21, 2025Expired
Registration details
Analysis ID
3b4e9001a539b60f38dbc2f10098e773
License Form
Ministry of Health Medical Device Import No. 022052
Customs Code
DHA09402205201
Company information
Manufacturer Country
Germany
Authorized Representative
AESOLUTION BIOMEDICAL CO. LTD.
Product details
Intended Use
Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Manual Instruments for General Surgery (I.4800)".
Product Type (Level 1)
I General and plastic surgical devices
Product Type (Level 2)
I4800 General Surgery Manual Instrument
Import Information
Imported from abroad
Dates and status
Registration Date
Oct 21, 2020
Expiry Date
Oct 21, 2025
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About this record

Access comprehensive regulatory information for "Asclepion" Manual surgical instrument for general use (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 3b4e9001a539b60f38dbc2f10098e773 and manufactured by Asclepion Laser Technologies GmbH. The authorized representative in Taiwan is AESOLUTION BIOMEDICAL CO. LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Asclepion Laser Technologies GmbH, and 2 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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