Taiwan FDA registration 3377fdc8a35c5d3a62ee2228ad1f54d3

"Dark" pathology diagnosis of glandular tumor markers with primary antibodies (unsterilized)

TW: "達克" 病理診斷腺腫瘤標記用一級抗體 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·Agilent Technologies, Inc.·Registered Dec 21, 2011 – Dec 21, 2026Active
Registration details
Analysis ID
3377fdc8a35c5d3a62ee2228ad1f54d3
Customs Code
DHA04401116408
Company information
Manufacturer Country
United States
Authorized Representative
SCN TRADING COMPANY LIMITED
Product details
Intended Use
Limit the classification and grading management of medical equipment "immunopathological histochemical reagents and sets (B.1860) the first level identification range.
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
Dec 21, 2011
Expiry Date
Dec 21, 2026
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About this record

Access comprehensive regulatory information for "Dark" pathology diagnosis of glandular tumor markers with primary antibodies (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 3377fdc8a35c5d3a62ee2228ad1f54d3 and manufactured by Agilent Technologies, Inc.. The authorized representative in Taiwan is SCN TRADING COMPANY LIMITED.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Agilent Technologies Denmark ApS., 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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