Taiwan FDA registration 54885a6a2a4c89588d85d0cd2a2a6316

Manual surgical instruments (unsterilized)

TW: "芮柏芙" 手動式外科器械 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·ZEPF MEDICAL INSTRUMENTS GMBH·Registered Feb 08, 2012 – Feb 08, 2022Cancelled
Registration details
Analysis ID
54885a6a2a4c89588d85d0cd2a2a6316
Customs Code
DHA04401135107
Company information
Manufacturer Country
Germany
Authorized Representative
HIGH TOP MEDICAL 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, Plastic Surgery and Dermatology
Product Type (Level 2)
I.4800 Hand Instruments for General Surgery
Import Information
import
Dates and status
Registration Date
Feb 08, 2012
Expiry Date
Feb 08, 2022
Cancellation Date
Apr 12, 2024
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 Manual surgical instruments (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 54885a6a2a4c89588d85d0cd2a2a6316 and manufactured by ZEPF MEDICAL INSTRUMENTS GMBH. The authorized representative in Taiwan is HIGH TOP MEDICAL CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 5 companies making similar products including G. ALBERT STORZ, GRACE MEDICAL, INC., and 5 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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