Taiwan FDA registration a1ebe06bafef5d84a549f789b8e205e1
"Intra-Lock" Capillary Blood Collection Tube (Non-Sterile)
TW: "英德樂可" 毛細管血液收集管 (未滅菌)
Taiwan·Risk Class 1·MD·INTRA-LOCK, INTERNATIONAL, INC.·Registered Oct 16, 2014 – Oct 16, 2019CancelledRegistration details
- Analysis ID
- a1ebe06bafef5d84a549f789b8e205e1
- License Form
- Ministry of Health Medical Device Import No. 014581
- Customs Code
- DHA09401458106
Company information
- Manufacturer
- INTRA-LOCK, INTERNATIONAL, INC.
- Manufacturer Country
- United States
- Authorized Representative
- HONG YANG BIOTECHNOLOGY CO., LTD.
Product details
- Product Type (Level 1)
- B Hematology and pathology devices
- Product Type (Level 2)
- B6150 Capillary blood collection tube
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Oct 16, 2014
- Expiry Date
- Oct 16, 2019
- 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 "Intra-Lock" Capillary Blood Collection Tube (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 a1ebe06bafef5d84a549f789b8e205e1 and manufactured by INTRA-LOCK, INTERNATIONAL, INC.. The authorized representative in Taiwan is HONG YANG BIOTECHNOLOGY CO., LTD..
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