Taiwan FDA registration 1e658dbfae2e0872f91898144c4b1860

"Wonder" skull plate anvil (unsterilized)

TW: “萬德”顱骨板鐵砧 (未滅菌)

Taiwan·Risk Class 1·Wande Disabled Equipment Co., Ltd. Zhonghe Factory·Registered Jan 04, 2008 – Jan 04, 2018Cancelled

Registration details

Analysis ID: 1e658dbfae2e0872f91898144c4b1860

Company information

Manufacturer: Wande Disabled Equipment Co., Ltd. Zhonghe Factory
Manufacturer Country: Taiwan, Province of China
Authorized Representative: WAN DER DIABLED PERSON'S AID & SUPPLIES. CO., LTD.

Product details

Intended Use: Limited to the first level of identification of skull plate anvil (K.4030) of the Measures for the Administration of Medical Devices.
Product Type (Level 1): K Neuroscience
Product Type (Level 2): K.4030 Skullbone plate anvil
Import Information: Domestic

Dates and status

Registration Date: Jan 04, 2008
Expiry Date: Jan 04, 2018
Cancellation Date: Nov 15, 2019

Cancellation information

Status: Logged out
Reason: 許可證已逾有效期

About this record

Access comprehensive regulatory information for "Wonder" skull plate anvil (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 1e658dbfae2e0872f91898144c4b1860 and manufactured by Wande Disabled Equipment Co., Ltd. Zhonghe Factory. The authorized representative in Taiwan is WAN DER DIABLED PERSON'S AID & SUPPLIES. CO., LTD..

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