Taiwan FDA registration 6a1427e5ab8556062254fe6779bca872
"Ulti med" Ovulations - Test (Non-Sterile)
TW: "爾提美" 排卵試劑 (未滅菌)
Taiwan·Risk Class 1·MD·ULTI MED PRODUCTS (DEUTSCHLAND) GMBH·Registered Nov 03, 2014 – Nov 03, 2019CancelledRegistration details
- Analysis ID
- 6a1427e5ab8556062254fe6779bca872
- License Form
- Ministry of Health Medical Device Import No. 014626
- Customs Code
- DHA09401462602
Company information
- Manufacturer
- ULTI MED PRODUCTS (DEUTSCHLAND) GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- BioChain Co., Ltd.
Product details
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A1485 Luteinizing Gonadotropin Test System
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Nov 03, 2014
- Expiry Date
- Nov 03, 2019
- Cancellation Date
- Jun 16, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期未申請展延
About this record
Access comprehensive regulatory information for "Ulti med" Ovulations - 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 6a1427e5ab8556062254fe6779bca872 and manufactured by ULTI MED PRODUCTS (DEUTSCHLAND) GMBH. The authorized representative in Taiwan is BioChain Co., Ltd..
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