Taiwan FDA registration 9438a3ccf51524c3ac0e7e8c3c6ce17e

"Met" Sharp Cannula System (Sterilization)

TW: “邁特”可利套管系統(滅菌)
Taiwan flagTaiwan·Risk Class 1·DEPUY MITEK, A JOHNSON & JOHNSON COMPANY·Registered Oct 20, 2008 – Oct 20, 2013Cancelled
Registration details
Analysis ID
9438a3ccf51524c3ac0e7e8c3c6ce17e
Customs Code
DHA04400714301
Company information
Manufacturer Country
United States
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
QMS/QSD;; 輸入
Dates and status
Registration Date
Oct 20, 2008
Expiry Date
Oct 20, 2013
Cancellation Date
Sep 26, 2016
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 "Met" Sharp Cannula System (Sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 9438a3ccf51524c3ac0e7e8c3c6ce17e and manufactured by DEPUY MITEK, A JOHNSON & JOHNSON COMPANY. The authorized representative in Taiwan is Yingshang Zhuangsheng and Zhuangsheng (Hong Kong) Co., Ltd. Taiwan Branch.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including DEPUY MITEK, A JOHNSON & JOHNSON COMPANY;; 大瓏企業股份有限公司, 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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