Taiwan FDA registration a6c9c6cd20865f439c90cc892f95dd63

"AccuroDesign" Cranioplasty material forming module (Non-Sterile)

TW: "德祁" 頭顱造型術材料形成模具 (未滅菌)

Taiwan·Risk Class 1·MD·AccuroDesign technology Inc.·Registered Apr 29, 2020 – Apr 29, 2025Expired

Registration details

Analysis ID: a6c9c6cd20865f439c90cc892f95dd63
License Form: Ministry of Health Medical Device Manufacturing No. 008302

Company information

Manufacturer: AccuroDesign technology Inc.
Manufacturer Country: Taiwan, Province of China
Authorized Representative: AccuroDesign technology Inc.

Product details

Intended Use: Limited to the first level identification range of the Measures for the Administration of Medical Devices "Material Formation Tools for Craniomodeling (K.4500)".
Product Type (Level 1): K Devices for neuroscience
Product Type (Level 2): K4500 Material formation tool for cranial modeling
Import Information: Produced in Taiwan, China

Dates and status

Registration Date: Apr 29, 2020
Expiry Date: Apr 29, 2025

About this record

Access comprehensive regulatory information for "AccuroDesign" Cranioplasty material forming module (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 a6c9c6cd20865f439c90cc892f95dd63 and manufactured by AccuroDesign technology Inc.. The authorized representative in Taiwan is AccuroDesign technology Inc..

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