Taiwan FDA registration 2f7d4942ad45477c7303bb775a231775
"MP" hGH Test (Non-Sterile)
TW: "馬丁彼得" 人類生長激素檢驗試劑 (未滅菌)
Taiwan·Risk Class 1·MD·MP BIOMEDICALS DIAGNOSTICS DIVISION·Registered Jul 21, 2014 – Jul 21, 2024ExpiredRegistration details
- Analysis ID
- 2f7d4942ad45477c7303bb775a231775
- License Form
- Ministry of Health Medical Device Import No. 014346
- Customs Code
- DHA09401434609
Company information
- Manufacturer
- MP BIOMEDICALS DIAGNOSTICS DIVISION
- Manufacturer Country
- United States
- Authorized Representative
- GENERAL BIOLOGICALS CORP.
Product details
- Intended Use
- Limited to the first level identification range of the human growth hormone test system (A.1370) of the management measures for medical equipment.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A1370 Human Growth Hormone Test System
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jul 21, 2014
- Expiry Date
- Jul 21, 2024
About this record
Access comprehensive regulatory information for "MP" hGH Test (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 2f7d4942ad45477c7303bb775a231775 and manufactured by MP BIOMEDICALS DIAGNOSTICS DIVISION. The authorized representative in Taiwan is GENERAL BIOLOGICALS CORP..
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