Taiwan FDA registration 26df966c6cf6e224b25b73d0e45e19d3
Pursen luteinizing hormone (unsterilized)
TW: 普生黃體促素(未滅菌)
Taiwan·Risk Class 1·MP BIOMEDICALS DIAGNOSTICS DIVISION·Registered Sep 22, 2005 – Sep 22, 2020CancelledRegistration details
- Analysis ID
- 26df966c6cf6e224b25b73d0e45e19d3
- Customs Code
- DHAS4400055000
Company information
- Manufacturer
- MP BIOMEDICALS DIAGNOSTICS DIVISION
- Manufacturer Country
- United States
- Authorized Representative
- GENERAL BIOLOGICALS CORP.
Product details
- Intended Use
- An extracorporeal diagnostic test to quantify the amount of yellow hormone in human serum or blood.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1485 Progesterone testing system
- Import Information
- Input;; Consent letter must be attached to the import (consent from the Atomic Energy Commission must be obtained for each import)
Dates and status
- Registration Date
- Sep 22, 2005
- Expiry Date
- Sep 22, 2020
- Cancellation Date
- Jul 15, 2022
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for Pursen luteinizing hormone (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 26df966c6cf6e224b25b73d0e45e19d3 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.
Free DatabasePowered by Pure Global AI89,000+ Devices