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"ORTHOPLI" DENTAL HAND INSTRUMENT (Non-Sterile) - Taiwan Registration 461229b00f1b759be480a19e06dca871

Access comprehensive regulatory information for "ORTHOPLI" DENTAL HAND INSTRUMENT (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 461229b00f1b759be480a19e06dca871 and manufactured by ORTHOPLI CORPORATION. The authorized representative in Taiwan is A & J BROS. TRADING CO., LTD..

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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461229b00f1b759be480a19e06dca871
Registration Details
Taiwan FDA Registration: 461229b00f1b759be480a19e06dca871
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Device Details

"ORTHOPLI" DENTAL HAND INSTRUMENT (Non-Sterile)
TW: "ๆญ็‘Ÿ่Š" ็‰™็ง‘ๆ‰‹็”จๅ™จๆขฐ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

461229b00f1b759be480a19e06dca871

Ministry of Health Medical Device Import No. 018182

DHA09401818202

Company Information

United States

Product Details

Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Dental Hand Instruments (F.4565)".

F Dental devices

F4565 Hand instruments for dental use

Imported from abroad

Dates and Status

Aug 11, 2017

Aug 11, 2022