Taiwan FDA registration 21278ede74a1157f402440bf07623263
"Kemel" syringe rack (unsterilized)
TW: “可美爾” 注射架 (未滅菌)
Taiwan·Risk Class 1·CARMEL PHARMA AB·Registered Jun 09, 2010 – Jun 09, 2015CancelledRegistration details
- Analysis ID
- 21278ede74a1157f402440bf07623263
- Customs Code
- DHA04400889001
Company information
- Manufacturer
- CARMEL PHARMA AB
- Manufacturer Country
- Sweden
- Authorized Representative
- MEDFRONT MEDICAL TECHNOLOGY CORPORATION
Product details
- Intended Use
- Limited to the first level identification range of the "Injection Rack (J.6990)" of the Measures for the Administration of Medical Equipment.
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J.6990 Injection holder
- Import Information
- import
Dates and status
- Registration Date
- Jun 09, 2010
- Expiry Date
- Jun 09, 2015
- Cancellation Date
- Jul 02, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Kemel" syringe rack (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 21278ede74a1157f402440bf07623263 and manufactured by CARMEL PHARMA AB. The authorized representative in Taiwan is MEDFRONT MEDICAL TECHNOLOGY CORPORATION.
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