Taiwan FDA registration 6bd7ba41ec5ac6201cd8f47fb749867f

"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 May 05, 2006 – May 05, 2021Cancelled
Registration details
Analysis ID
6bd7ba41ec5ac6201cd8f47fb749867f
Customs Code
DHA04400437201
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
import
Dates and status
Registration Date
May 05, 2006
Expiry Date
May 05, 2021
Cancellation Date
May 06, 2019
Cancellation information
Status
Logged out
Reason
自行鍵入
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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 6bd7ba41ec5ac6201cd8f47fb749867f 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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