Taiwan FDA registration 2592c2a8b12ec673fbbb1f290600ddd0
"TAI TSANG" TUBE SEALER (NON-STERILE)
TW: "泰瑲" 血袋封口機 (未滅菌)
Taiwan·Risk Class 1·MD·LJUNGBERG & KOGEL AB·Registered May 15, 2015 – May 15, 2020CancelledRegistration details
- Analysis ID
- 2592c2a8b12ec673fbbb1f290600ddd0
- License Form
- Ministry of Health Medical Device Import No. 015223
- Customs Code
- DHA09401522301
Company information
- Manufacturer
- LJUNGBERG & KOGEL AB
- Manufacturer Country
- Sweden
- Authorized Representative
- TAI TSANG TECHNOLOGY CORP.
Product details
- Product Type (Level 1)
- B Hematology and pathology devices
- Product Type (Level 2)
- B9750 Heat sealing equipment
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- May 15, 2015
- Expiry Date
- May 15, 2020
- Cancellation Date
- Aug 05, 2022
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "TAI TSANG" TUBE SEALER (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 2592c2a8b12ec673fbbb1f290600ddd0 and manufactured by LJUNGBERG & KOGEL AB. The authorized representative in Taiwan is TAI TSANG TECHNOLOGY CORP..
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