Taiwan FDA registration 7aca43060c8a4b7ec3b57584f60057b8

"Roche" insulin growth factor type 1 receptor probe (unsterilized)

TW: “羅氏”類胰島素生長因子一型受體探針(未滅菌)

Taiwan·Risk Class 1·ROCHE DIAGNOSTICS GMBH;; VENTANA MEDICAL SYSTEMS, INC.·Registered Aug 22, 2011 – Aug 22, 2016Cancelled

Registration details

Analysis ID: 7aca43060c8a4b7ec3b57584f60057b8
Customs Code: DHA04401073405

Company information

Manufacturer: ROCHE DIAGNOSTICS GMBH;; VENTANA MEDICAL SYSTEMS, INC.
Manufacturer Country: United States;;Germany
Authorized Representative: ROCHE DIAGNOSTICS LTD.

Product details

Intended Use: Limited to the first level identification range of immunopathological histochemical reagents and kits (B.1860) of the Measures for the Administration of Medical Devices.
Product Type (Level 1): B Hematology, pathology, and genetics
Product Type (Level 2): B.1860 Immunopathological histochemistry reagents and kits
Import Information: import

Dates and status

Registration Date: Aug 22, 2011
Expiry Date: Aug 22, 2016
Cancellation Date: May 28, 2018

Cancellation information

Status: Logged out
Reason: 許可證已逾有效期

About this record

Access comprehensive regulatory information for "Roche" insulin growth factor type 1 receptor probe (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 7aca43060c8a4b7ec3b57584f60057b8 and manufactured by ROCHE DIAGNOSTICS GMBH;; VENTANA MEDICAL SYSTEMS, INC.. The authorized representative in Taiwan is ROCHE DIAGNOSTICS 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.