Taiwan FDA registration 97d1c62b3d9677e0847d0f4b67597d08

"Artre" surgical instruments, motors and accessories or accessories (unsterilized)

TW: "阿特爾"手術用器具馬達與配件或附件(未滅菌)

Taiwan·Risk Class 1·ALTAIR INSTRUMENTS INC.·Registered Aug 16, 2011 – Aug 16, 2021Cancelled

Registration details

Analysis ID: 97d1c62b3d9677e0847d0f4b67597d08
Customs Code: DHA04401070906

Company information

Manufacturer: ALTAIR INSTRUMENTS INC.
Manufacturer Country: United States
Authorized Representative: NEOASIA LTD.

Product details

Intended Use: Limited to the first level of identification scope of the Measures for the Administration of Medical Devices "Surgical Instruments, Motors and Accessories or Accessories (I.4820)".
Product Type (Level 1): I General, Plastic Surgery and Dermatology
Product Type (Level 2): I.4820 Surgical Appliances and Accessories or Accessories
Import Information: import

Dates and status

Registration Date: Aug 16, 2011
Expiry Date: Aug 16, 2021
Cancellation Date: Oct 12, 2023

Cancellation information

Status: Logged out
Reason: 未展延而逾期者

About this record

Access comprehensive regulatory information for "Artre" surgical instruments, motors and accessories or accessories (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 97d1c62b3d9677e0847d0f4b67597d08 and manufactured by ALTAIR INSTRUMENTS INC.. The authorized representative in Taiwan is NEOASIA LTD..

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