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Sergipas smear fixative (unsterilized) - Taiwan Registration 8b80d04aaa4c6ea611832bbb3321361d

Access comprehensive regulatory information for Sergipas smear fixative (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 8b80d04aaa4c6ea611832bbb3321361d and manufactured by SURGIPATH MEDICAL INDUSTRIES, INC.. The authorized representative in Taiwan is MIN JIER FIRM.

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.

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8b80d04aaa4c6ea611832bbb3321361d
Registration Details
Taiwan FDA Registration: 8b80d04aaa4c6ea611832bbb3321361d
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Device Details

Sergipas smear fixative (unsterilized)
TW: ็‘Ÿๅ‰ๅธ•ๆ–ฏๆŠน็‰‡ๅ›บๅฎšๆถฒ(ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

8b80d04aaa4c6ea611832bbb3321361d

DHA04400550305

Company Information

United States

Product Details

Limited to the first level identification scope of "General Purpose Reaction Reagents (B.4010)" under the Measures for the Administration of Medical Devices.

B Hematology, pathology, and genetics

B.4010 Reaction Reagents for General Purposes

import

Dates and Status

Jan 08, 2007

Jan 08, 2017

Dec 05, 2019

Cancellation Information

Logged out

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