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BECKMAN COULTER IGF-I IRMA Kit - Taiwan Registration e5f8c155ed6eca7cc24146dfd2d8413a

Access comprehensive regulatory information for BECKMAN COULTER IGF-I IRMA Kit in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e5f8c155ed6eca7cc24146dfd2d8413a and manufactured by IMMUNOTECH S.R.O.. The authorized representative in Taiwan is BECKMAN COULTER TAIWAN INC., TAIWAN BRANCH (U.S.A.).

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e5f8c155ed6eca7cc24146dfd2d8413a
Registration Details
Taiwan FDA Registration: e5f8c155ed6eca7cc24146dfd2d8413a
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Device Details

BECKMAN COULTER IGF-I IRMA Kit
TW: ่ฒๅ…‹ๆ›ผๅบซ็ˆพ็‰น่ƒฐๅณถ็ด ็”Ÿ้•ทๅ› ๅญ็ฌฌไธ€ๅž‹ๆ”พๅฐ„ๅ…็–ซๅˆ†ๆž่ฉฆๅŠ‘็ต„
Risk Class 2
MD

Registration Details

e5f8c155ed6eca7cc24146dfd2d8413a

Ministry of Health Medical Device Import No. 028432

DHAS5602843203

Company Information

Product Details

In vitro quantification of insulin growth factor type 1 in human serum and plasma using radioimmunoassay.

A Clinical chemistry and clinical toxicology

A1370 Human Growth Hormone Test System

Imported from abroad; Consent must be attached to the input (each input must be supported by the consent of the Atomic Energy Commission)

Dates and Status

May 26, 2016

May 26, 2026