Taiwan FDA registration a95d7c67d0b3ace5c8892c4fd4f04ae2
“Boditech” Hemochroma PLUS
TW: "波狄塔克"血紅素測量系統
Taiwan·Risk Class 2·MD·Boditech Med Inc.·Registered Jan 14, 2020 – Jan 14, 2025ExpiredRegistration details
- Analysis ID
- a95d7c67d0b3ace5c8892c4fd4f04ae2
- License Form
- Ministry of Health Medical Device Import No. 033132
- Customs Code
- DHA05603313203
Company information
- Manufacturer
- Boditech Med Inc.
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- Y.H. BIOTEK CO., LTD.
Product details
- Intended Use
- This product is a portable in vitro diagnostic instrument used to measure the heme value in the blood.
- Product Type (Level 1)
- B Hematology and pathology devices
- Product Type (Level 2)
- B5620 Automated Heme Analysis System
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jan 14, 2020
- Expiry Date
- Jan 14, 2025
About this record
Access comprehensive regulatory information for “Boditech” Hemochroma PLUS in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a95d7c67d0b3ace5c8892c4fd4f04ae2 and manufactured by Boditech Med Inc.. The authorized representative in Taiwan is Y.H. BIOTEK CO., LTD..
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