Taiwan FDA registration b1037a9b3e9b0c19f849c72db6312aa7

"Spite" Manual Orthopedic Surgical Instruments (Unsterilized)

TW: "斯佰特" 手動式骨科手術器械 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·SPINEART SA·Registered Feb 24, 2012 – Feb 24, 2017Cancelled
Registration details
Analysis ID
b1037a9b3e9b0c19f849c72db6312aa7
Customs Code
DHA04401141201
Company information
Manufacturer
SPINEART SA
Manufacturer Country
Switzerland
Authorized Representative
RISES THAI BIOTECH LIMITED
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
Feb 24, 2012
Expiry Date
Feb 24, 2017
Cancellation Date
Nov 15, 2019
Cancellation information
Status
Logged out
Reason
許可證已逾有效期
About this record

Access comprehensive regulatory information for "Spite" Manual Orthopedic 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 b1037a9b3e9b0c19f849c72db6312aa7 and manufactured by SPINEART SA. The authorized representative in Taiwan is RISES THAI BIOTECH LIMITED.

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