Taiwan FDA registration dc18efd72a008b29706cca6b63e5c859

"Zhuangsheng" Vijo sutures

TW: "壯生"薇喬縫合線
Taiwan flagTaiwan·Risk Class 2·Johnson & Johnson International, c/o European Logistics Centre;; JOHNSON & JOHNSON MEDICAL LIMITED·Registered Jan 16, 2007 – Jan 16, 2022Cancelled
Registration details
Analysis ID
dc18efd72a008b29706cca6b63e5c859
Customs Code
DHA00601768902
Company information
Manufacturer Country
United Kingdom;;Belgium
Authorized Representative
JOHNSON & JOHNSON MEDICAL TAIWAN LTD.
Product details
Intended Use
For details, it is Chinese approved copy of the imitation order
Product Type (Level 1)
I General, Plastic Surgery and Dermatology
Product Type (Level 2)
I.4493 Absorbable crossover ester surgical sewing thread
Import Information
import
Dates and status
Registration Date
Jan 16, 2007
Expiry Date
Jan 16, 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 "Zhuangsheng" Vijo sutures in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number dc18efd72a008b29706cca6b63e5c859 and manufactured by Johnson & Johnson International, c/o European Logistics Centre;; JOHNSON & JOHNSON MEDICAL LIMITED. The authorized representative in Taiwan is JOHNSON & JOHNSON MEDICAL TAIWAN LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including JOHNSON & JOHNSON MEDICAL GMBH;; Johnson & Johnson International, c/o European Logistics Centre, 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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