Taiwan FDA registration ed9c371a06d24f695478d7a7cd70e34f

Aushi Ammycin 30 mcg paper ingots

TW: 傲世 安黴素30微克紙錠
Taiwan flagTaiwan·Risk Class 2·OXOID LIMITED·Registered Mar 15, 2006 – Mar 15, 2011Cancelled
Registration details
Analysis ID
ed9c371a06d24f695478d7a7cd70e34f
Customs Code
DHA00601615002
Company information
Manufacturer
OXOID LIMITED
Manufacturer Country
United Kingdom
Authorized Representative
Qixin Biotechnology Co., Ltd
Product details
Intended Use
It is used as an antibiotic susceptibility test for amphecline.
Product Type (Level 1)
C Immunology and microbiology
Product Type (Level 2)
C.1620 抗菌感受性試驗盤
Import Information
import
Dates and status
Registration Date
Mar 15, 2006
Expiry Date
Mar 15, 2011
Cancellation Date
Nov 08, 2012
Cancellation information
Status
Logged out
Reason
許可證已逾有效期
About this record

Access comprehensive regulatory information for Aushi Ammycin 30 mcg paper ingots in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ed9c371a06d24f695478d7a7cd70e34f and manufactured by OXOID LIMITED. The authorized representative in Taiwan is Qixin Biotechnology 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.

Free DatabasePowered by Pure Global AI89,000+ Devices