Taiwan FDA registration 8dddeadb8c5c4ee7499528aaf5d4c567

"Lianchuang Aikaifu" vertebroplasty bone cement

TW: “聯創愛凱福”椎體成形術骨水泥

Taiwan·Risk Class 2·Taiwan MicroPort Medical Equipment Co., Ltd. Zhubei Factory·Registered Mar 03, 2023 – Feb 12, 2025Expired

Registration details

Analysis ID: 8dddeadb8c5c4ee7499528aaf5d4c567

Company information

Manufacturer: Taiwan MicroPort Medical Equipment Co., Ltd. Zhubei Factory
Manufacturer Country: Taiwan, Province of China
Authorized Representative: Lianchuang Biomedical Co., Ltd

Product details

Intended Use: Details are as detailed as approved Chinese instructions
Product Type (Level 1): N Orthopedics
Product Type (Level 2): N.3027 PMMA骨水泥
Import Information: Domestic;; Contract manufacturing

Dates and status

Registration Date: Mar 03, 2023
Expiry Date: Feb 12, 2025

About this record

Access comprehensive regulatory information for "Lianchuang Aikaifu" vertebroplasty bone cement in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 8dddeadb8c5c4ee7499528aaf5d4c567 and manufactured by Taiwan MicroPort Medical Equipment Co., Ltd. Zhubei Factory. The authorized representative in Taiwan is Lianchuang Biomedical Co., Ltd.

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