Martin Peter Estradiol Hormone Diagnostic Kit
- Analysis ID
- 1970f04364215c95ad42ec4994094b4a
- Customs Code
- DHAS5602954304
- Manufacturer
- MP BIOMEDICALS DIAGNOSTICS DIVISION
- Manufacturer Country
- United States
- Authorized Representative
- GENERAL BIOLOGICALS CORP.
- Intended Use
- Quantitative detection of estradiol hormone in human serum or plasma.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1260 雌二醇試驗系統
- Import Information
- Input;; Consent letter must be attached to the import (consent from the Atomic Energy Commission must be obtained for each import)
- Registration Date
- Apr 14, 2017
- Expiry Date
- Apr 14, 2027
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Access comprehensive regulatory information for Martin Peter Estradiol Hormone Diagnostic Kit in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 1970f04364215c95ad42ec4994094b4a and manufactured by MP BIOMEDICALS DIAGNOSTICS DIVISION. The authorized representative in Taiwan is GENERAL BIOLOGICALS CORP..
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