Taiwan FDA registration cca9a77daa79364502acf93dfb86f9f7

MP Prolactin CT

TW: 馬丁彼得泌乳激素診斷套組

Taiwan·Risk Class 2·MD·MP Biomedicals Diagnostics Division·Registered Mar 29, 2017 – Mar 29, 2022Expired

Registration details

Analysis ID: cca9a77daa79364502acf93dfb86f9f7
License Form: Ministry of Health Medical Device Import No. 029525
Customs Code: DHAS5602952502

Company information

Manufacturer: MP Biomedicals Diagnostics Division
Manufacturer Country: United States
Authorized Representative: GENERAL BIOLOGICALS CORP.

Product details

Intended Use: This product is a radioimmunoassay for the in vitro quantification of human serum prolactin.
Product Type (Level 1): A Clinical chemistry and clinical toxicology
Product Type (Level 2): A1625 Prolactin Test System
Import Information: 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

Registration Date: Mar 29, 2017
Expiry Date: Mar 29, 2022

About this record

Access comprehensive regulatory information for MP Prolactin CT in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number cca9a77daa79364502acf93dfb86f9f7 and manufactured by MP Biomedicals Diagnostics Division. The authorized representative in Taiwan is GENERAL BIOLOGICALS CORP..

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.