Taiwan FDA registration 6483c612f6ead0b5bf8c27abba169b60
"Lehau" Erma blood analysis system
TW: “萊豪” 爾瑪血液分析系統
Taiwan·Risk Class 2·LifeHealth·Registered Nov 27, 2017 – Nov 27, 2022CancelledRegistration details
- Analysis ID
- 6483c612f6ead0b5bf8c27abba169b60
- Customs Code
- DHA05603046301
Company information
- Manufacturer
- LifeHealth
- Manufacturer Country
- United States
- Authorized Representative
- BEAM INTERNATIONAL INC.
Product details
- Intended Use
- This product is paired with an IRMA TRUPoint cartridge for professionals to use in whole blood analysis.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1120 血內氣體(PCO2,PO2)及血液pH值試驗系統;; A.1145 鈣試驗系統;; A.1160 重碳酸鹽/二氧化碳試驗系統
- Import Information
- import
Dates and status
- Registration Date
- Nov 27, 2017
- Expiry Date
- Nov 27, 2022
- Cancellation Date
- Apr 12, 2024
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Lehau" Erma blood analysis system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 6483c612f6ead0b5bf8c27abba169b60 and manufactured by LifeHealth. The authorized representative in Taiwan is BEAM INTERNATIONAL INC..
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