Taiwan FDA registration b75f9d8c3cfc2e512a93a478834cf632
"SAR" SAREVAC BODY SPLINT (Non-Sterile)
TW: "莎爾" 伊貝克捲式擔架 (未滅菌)
Taiwan·Risk Class 1·MD·SAR PRODUCTS LTD. (SPECIALIST ACCESS & RESCUE PRODUCTS LTD)·Registered Mar 06, 2015 – Mar 06, 2020CancelledRegistration details
- Analysis ID
- b75f9d8c3cfc2e512a93a478834cf632
- License Form
- Ministry of Health Medical Device Import No. 014970
- Customs Code
- DHA09401497004
Company information
- Manufacturer Country
- United Kingdom
- Authorized Representative
- REPUTATION AND PROSPERITY CO., LTD.
Product details
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J6900 portable stretcher
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Mar 06, 2015
- Expiry Date
- Mar 06, 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 "SAR" SAREVAC BODY SPLINT (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 b75f9d8c3cfc2e512a93a478834cf632 and manufactured by SAR PRODUCTS LTD. (SPECIALIST ACCESS & RESCUE PRODUCTS LTD). The authorized representative in Taiwan is REPUTATION AND PROSPERITY CO., LTD..
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