Taiwan FDA registration c7485c2c579f071cf388b91d86aaed5e
"ULTI MED" LH Ovulation Test (Non-Sterile)
TW: "爾媞美"排卵檢測試劑 (未滅菌)
Taiwan·Risk Class 1·MD·ULTI MED PRODUCTS (DEUTSCHLAND) GMBH·Registered Feb 05, 2021 – Feb 05, 2026ExpiredRegistration details
- Analysis ID
- c7485c2c579f071cf388b91d86aaed5e
- License Form
- Ministry of Health Medical Device Import No. 022302
- Customs Code
- DHA09402230201
Company information
- Manufacturer
- ULTI MED PRODUCTS (DEUTSCHLAND) GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- BioChain Co., Ltd.
Product details
- Intended Use
- Limited to the first level recognition range of the "Luteinizing hormone test system (A.1485)" of the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A1485 Progesterone Test System
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Feb 05, 2021
- Expiry Date
- Feb 05, 2026
About this record
Access comprehensive regulatory information for "ULTI MED" LH Ovulation 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 c7485c2c579f071cf388b91d86aaed5e and manufactured by ULTI MED PRODUCTS (DEUTSCHLAND) GMBH. The authorized representative in Taiwan is BioChain Co., Ltd..
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