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"BOTTEN" dental surgery light (unsterilized) - Taiwan Registration dfc06d0a8b88e9c284c8a1629a2028c7

Access comprehensive regulatory information for "BOTTEN" dental surgery light (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number dfc06d0a8b88e9c284c8a1629a2028c7 and manufactured by BURTON MEDICAL PRODUCTS CORPORATION. The authorized representative in Taiwan is KINGJING INTERNATIONAL CO., LTD..

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dfc06d0a8b88e9c284c8a1629a2028c7
Registration Details
Taiwan FDA Registration: dfc06d0a8b88e9c284c8a1629a2028c7
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Device Details

"BOTTEN" dental surgery light (unsterilized)
TW: "ๅš้จฐ"็‰™็ง‘ๆ‰‹่ก“็‡ˆ(ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

dfc06d0a8b88e9c284c8a1629a2028c7

DHA04401038009

Company Information

United States

Product Details

Limited to the first level recognition range of the Measures for the Administration of Medical Equipment "Dental Surgical Light (F.4630)".

F Dentistry

F.4630 ็‰™็ง‘็”จๆ‰‹่ก“็‡ˆ

import

Dates and Status

May 20, 2011

May 20, 2016

Jun 26, 2018

Cancellation Information

Logged out

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