Taiwan FDA registration 945cd81fe60bd341417afb10abebcc0a

"Sindis" manual orthopedic surgical instruments (sterile/unsterilized)

TW: “信迪思”手動式骨科手術器械(滅菌/未滅菌)
Taiwan flagTaiwan·Risk Class 1·SYNTHES GMBH·Registered Sep 13, 2018 – Sep 13, 2023Cancelled
Registration details
Analysis ID
945cd81fe60bd341417afb10abebcc0a
Customs Code
DHA09401959707
Company information
Manufacturer
SYNTHES GMBH
Manufacturer Country
Switzerland
Authorized Representative
JOHNSON & JOHNSON MEDICAL TAIWAN LTD.
Product details
Intended Use
Limited to the first level identification range of manual orthopedic surgical instruments (N.4540) of the Measures for the Administration of Medical Equipment.
Product Type (Level 1)
N Orthopedics
Product Type (Level 2)
N.4540 手動式骨科手術器械
Import Information
QMS/QSD;; 輸入
Dates and status
Registration Date
Sep 13, 2018
Expiry Date
Sep 13, 2023
Cancellation Date
May 25, 2020
Cancellation information
Status
Logged out
Reason
自請註銷
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About this record

Access comprehensive regulatory information for "Sindis" manual orthopedic surgical instruments (sterile/unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 945cd81fe60bd341417afb10abebcc0a and manufactured by SYNTHES GMBH. 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 SYNTHES GMBH, 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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