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Zhipeng Grinding device and its accessories (unsterilized) - Taiwan Registration d88fbd48491b91462ef82c728abb2550

Access comprehensive regulatory information for Zhipeng Grinding device and its 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 d88fbd48491b91462ef82c728abb2550 and manufactured by Penglin Enterprise Co., Ltd. Wanxing Factory. The authorized representative in Taiwan is Penglin Enterprise Co., Ltd. Wanxing Factory.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Penglin Enterprise Co., Ltd. Wanxing Factory, and 1 recent registrations in the same category. 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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d88fbd48491b91462ef82c728abb2550
Registration Details
Taiwan FDA Registration: d88fbd48491b91462ef82c728abb2550
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Device Details

Zhipeng Grinding device and its accessories (unsterilized)
TW: ๆ™บ้ตฌ ็ ”็ฃจ่ฃ็ฝฎๅŠๅ…ถ้™„ไปถ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

d88fbd48491b91462ef82c728abb2550

Company Information

Taiwan, Province of China

Product Details

Limited to the first level identification range of grinding devices and their accessories (F.6010) under the management measures for medical equipment.

F Dentistry

F.6010 Abrasive devices and accessories thereof

Domestic

Dates and Status

Jan 26, 2015

Jan 26, 2025

Sep 30, 2021

Cancellation Information

Logged out

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