Taiwan FDA registration ea568a0b260bc74b5492f0bc3cf3bad3

"Hiss" manual instruments for general surgery (unsterilized)

TW: "希司艾"一般手術用手動式器械(未滅菌)
Taiwan flagTaiwan·Risk Class 1·SPECIALTY SURGICAL INSTRUMENTATION·Registered Nov 23, 2012 – Nov 23, 2017Cancelled
Registration details
Analysis ID
ea568a0b260bc74b5492f0bc3cf3bad3
Customs Code
DHA04401239700
Company information
Manufacturer Country
United States
Authorized Representative
MATECH HEALTHCARE CORPORATION
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, Plastic Surgery and Dermatology
Product Type (Level 2)
I.4800 Hand Instruments for General Surgery
Import Information
import
Dates and status
Registration Date
Nov 23, 2012
Expiry Date
Nov 23, 2017
Cancellation Date
Nov 21, 2019
Cancellation information
Status
Logged out
Reason
未展延而逾期者
About this record

Access comprehensive regulatory information for "Hiss" manual instruments for general surgery (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number ea568a0b260bc74b5492f0bc3cf3bad3 and manufactured by SPECIALTY SURGICAL INSTRUMENTATION. The authorized representative in Taiwan is MATECH HEALTHCARE CORPORATION.

This page provides complete technical specifications, regulatory compliance details. 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.

Free DatabasePowered by Pure Global AI89,000+ Devices