Taiwan FDA registration 9e43a349d4e662e307508292fea09b4c

"Aceris" Arthroscopic Surgical Instruments Series (Unsterilized)

TW: "艾思瑞斯" 關節鏡手術用器械系列 (未滅菌)

Taiwan·Risk Class 1·ARTHREX INC.·Registered Oct 27, 2005 – Oct 27, 2010Cancelled

Registration details

Analysis ID: 9e43a349d4e662e307508292fea09b4c
Customs Code: DHA04400132602

Company information

Manufacturer: ARTHREX INC.
Manufacturer Country: United States
Authorized Representative: CHAWEI CO., LTD.

Product details

Intended Use: 協助關節鏡手術進行之手術器械,內容包含: 套管cannula, 刮匙curette鑽頭導引器dill guide, forceps鉗子, gouge鑿子, handle把手, knife刀子, sizer/temp裝填器, osteotome骨刀, probe探針, drill鑽孔器, rasp骨銼刀, retractor牽引器, punch骨鉗,縫線牽引器, knot pusher打結器, 剪線器scissor, reamer骨縫打孔器, rod控制桿及trocar套針.
Product Type (Level 1): N Orthopedics
Product Type (Level 2): N.1100 Closing Lenses
Import Information: import

Dates and status

Registration Date: Oct 27, 2005
Expiry Date: Oct 27, 2010
Cancellation Date: Nov 23, 2012

Cancellation information

Status: Logged out
Reason: 許可證已逾有效期

About this record

Access comprehensive regulatory information for "Aceris" Arthroscopic Surgical Instruments Series (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 9e43a349d4e662e307508292fea09b4c and manufactured by ARTHREX INC.. The authorized representative in Taiwan is CHAWEI CO., LTD..

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