Taiwan FDA registration 566929797c9c3d1ddcb93f29defa2745

"Apatek" Pentax Light Source and Accessories (Unsterilized)

TW: “阿帕泰克”賓得士光源及附件 (未滅菌)

Taiwan·Risk Class 1·APPLITEC LTD.·Registered Sep 01, 2006 – Sep 01, 2011Cancelled

Registration details

Analysis ID: 566929797c9c3d1ddcb93f29defa2745
Customs Code: DHA04400511203

Company information

Manufacturer: APPLITEC LTD.
Manufacturer Country: Israel
Authorized Representative: WHOLE WELL CO., LTD.

Product details

Intended Use: Limited to the first level identification scope of the Measures for the Administration of Medical Devices "ENT Fiber Optic Light Source and Vehicle (G.4350)".
Product Type (Level 1): G ENT Science
Product Type (Level 2): G.4350 Ear, nose and throat optical fiber light sources and carriers
Import Information: import

Dates and status

Registration Date: Sep 01, 2006
Expiry Date: Sep 01, 2011
Cancellation Date: Jul 25, 2014

Cancellation information

Status: Logged out
Reason: 許可證已逾有效期

About this record

Access comprehensive regulatory information for "Apatek" Pentax Light Source and 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 566929797c9c3d1ddcb93f29defa2745 and manufactured by APPLITEC LTD.. The authorized representative in Taiwan is WHOLE WELL CO., LTD..

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