Taiwan FDA registration c4c96c2d83fe67f036e378d10bd0194a

Selective medium (unsterilized)

TW: 〝利飛旋〞選擇性培養基(未滅菌)
Taiwan flagTaiwan·Risk Class 1·LIOFILCHEM S.R.L.·Registered Sep 05, 2011 – Sep 05, 2016Cancelled
Registration details
Analysis ID
c4c96c2d83fe67f036e378d10bd0194a
Customs Code
DHA04401080301
Company information
Manufacturer
LIOFILCHEM S.R.L.
Manufacturer Country
Italy
Authorized Representative
DYBO ENTERPRISE COMPANY LIMITED
Product details
Intended Use
Limited to the first level identification range of the Measures for the Administration of Medical Devices "Selective Media (C.2360)".
Product Type (Level 1)
C Immunology and microbiology
Product Type (Level 2)
C.2360 選擇性培養基
Import Information
import
Dates and status
Registration Date
Sep 05, 2011
Expiry Date
Sep 05, 2016
Cancellation Date
May 28, 2018
Cancellation information
Status
Logged out
Reason
許可證已逾有效期
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About this record

Access comprehensive regulatory information for Selective medium (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number c4c96c2d83fe67f036e378d10bd0194a and manufactured by LIOFILCHEM S.R.L.. The authorized representative in Taiwan is DYBO ENTERPRISE COMPANY LIMITED.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including BIOMERIEUX S.A., and 1 recent registrations in the same category. 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.

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