Taiwan FDA registration 207aef4f6d2bb69dbcc9994920ed9a35

Achipe buffered saline

TW: 艾視普緩衝生理食鹽水

Taiwan·Risk Class 2·TAIWAN BIOTECH CO., LTD.·Registered Jan 15, 2010 – May 18, 2017Cancelled

Registration details

Analysis ID: 207aef4f6d2bb69dbcc9994920ed9a35
Customs Code: DHY00500286704

Company information

Manufacturer: TAIWAN BIOTECH CO., LTD.
Manufacturer Country: Taiwan, Province of China
Authorized Representative: TAIWAN BIOTECH CO., LTD.

Product details

Intended Use: For details, it is Chinese approved copy of the imitation order
Product Type (Level 1): M Ophthalmology
Product Type (Level 2): M.5928 Products for the preservation of soft contact lenses
Import Information: Domestic

Dates and status

Registration Date: Jan 15, 2010
Expiry Date: May 18, 2017
Cancellation Date: Apr 11, 2017

Cancellation information

Status: Logged out
Reason: 自行鍵入

About this record

Access comprehensive regulatory information for Achipe buffered saline in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 207aef4f6d2bb69dbcc9994920ed9a35 and manufactured by TAIWAN BIOTECH CO., LTD.. The authorized representative in Taiwan is TAIWAN BIOTECH CO., LTD..

This page provides complete technical specifications, regulatory compliance details. 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.