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"Bausch" Occlusal analysis device & accessories (Non-sterile) - Taiwan Registration 32c5a6ec7219b754ac64c36d03f68519

Access comprehensive regulatory information for "Bausch" Occlusal analysis device & accessories (Non-sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 32c5a6ec7219b754ac64c36d03f68519 and manufactured by DR. JEAN BAUSCH GMBH & CO.KG. The authorized representative in Taiwan is E.S.T. BIOTECH INC..

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32c5a6ec7219b754ac64c36d03f68519
Registration Details
Taiwan FDA Registration: 32c5a6ec7219b754ac64c36d03f68519
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Device Details

"Bausch" Occlusal analysis device & accessories (Non-sterile)
TW: "ๆŸๆ–ฏ" ็‰™็ง‘ๅ’ฌๅˆๅˆ†ๆž่ฃ็ฝฎๅŠๅ…ถ้™„ไปถ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

32c5a6ec7219b754ac64c36d03f68519

Ministry of Health Medical Device Import Registration No. a00025

DHA084a0002500

Company Information

Germany

Product Details

Limited to the classification and grading management measures of medical equipment "occlusal paper (F.6140) first level identification range.

F Dentistry

F6140 Occlusal paper

Dates and Status

Nov 26, 2021

Oct 31, 2023