Taiwan FDA registration 318cbaad98ef0bb78721fd252d7e5344
"Instrumentation Laboratory" Capillary blood collection tube (Non-Sterile)
TW: "儀器實驗室" 毛細管血液收集管 (未滅菌)
Taiwan·Risk Class 1·MD·INSTRUMENTATION LABORATORY CO.·Registered Jan 28, 2019 – Jan 28, 2024ExpiredRegistration details
- Analysis ID
- 318cbaad98ef0bb78721fd252d7e5344
- License Form
- Ministry of Health Medical Device Import No. 020072
- Customs Code
- DHA09402007200
Company information
- Manufacturer
- INSTRUMENTATION LABORATORY CO.
- Manufacturer Country
- United States
- Authorized Representative
- Werfen Taiwan Limited
Product details
- Intended Use
- Limited to the first level identification range of "Capillary Blood Collection Tube (B.6150)" under the Measures for the Administration of Medical Devices.
- 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
- Jan 28, 2019
- Expiry Date
- Jan 28, 2024
About this record
Access comprehensive regulatory information for "Instrumentation Laboratory" 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 318cbaad98ef0bb78721fd252d7e5344 and manufactured by INSTRUMENTATION LABORATORY CO.. The authorized representative in Taiwan is Werfen Taiwan Limited.
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