Taiwan FDA registration b0c76653f1e310755d9ff2a7c4cbc3d2

“CHI SHENG” REFRESH CLEAN SOLUTION

TW: “濟生”芮視清沖洗液

Taiwan·Risk Class 2·MD·CHI SHENG PHARMA & BIOTECH CO., LTD·Registered Mar 15, 2016 – Mar 15, 2026Expired

Registration details

Analysis ID: b0c76653f1e310755d9ff2a7c4cbc3d2
License Form: Ministry of Health Medical Device Manufacturing No. 005275

Company information

Manufacturer: CHI SHENG PHARMA & BIOTECH CO., LTD
Manufacturer Country: Taiwan, Province of China
Authorized Representative: CHI SHENG PHARMA & BIOTECH CO., LTD

Product details

Intended Use: For details, it is Chinese approved copy of the imitation order
Product Type (Level 1): J General hospital and personal use equipment
Import Information: Produced in Taiwan, China

Dates and status

Registration Date: Mar 15, 2016
Expiry Date: Mar 15, 2026

About this record

Access comprehensive regulatory information for “CHI SHENG” REFRESH CLEAN SOLUTION in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b0c76653f1e310755d9ff2a7c4cbc3d2 and manufactured by CHI SHENG PHARMA & BIOTECH CO., LTD. The authorized representative in Taiwan is CHI SHENG PHARMA & BIOTECH CO., LTD.

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