Class 2 Device Recall Boston Scientific Scimed | 合法醫療器材資訊網
References
Related Medical Device
Recalls (www.accessdata.fda.gov)
P860019
(www.accessdata.fda.gov)
Catheters, Transluminal
Coronary Angioplasty, Percutaneous
(www.accessdata.fda.gov)
LOX
(www.accessdata.fda.gov)
TPLC Device Report
(www.accessdata.fda.gov)
medical device recalls
(www.fda.gov)
Code of Federal Regulations
(CFR) Title 21 §7.55
(www.accessdata.fda.gov)
PMAs with Product Code = LOX
and Original Applicant = SCIMED LIFE SYSTEMS, INC.
(www.accessdata.fda.gov)
Date Initiated by Firm
August 20, 2003
Date Posted
October 15, 2003
Recall Status1
...
"SCIMED" PTA CATHETER "SCIMED" PTA CATHETER 高登智慧科技深圳有限公司 Atellica CH Carbon Dioxide Concentrated GE Healthcare ge醫療器材 self-sealing capillary tubes plastic capillary tubes “Woodpecker” Heat source for bleaching teeth (Non-Sterile) "Ctu" Preformed crown (Non-Sterile)
Class 2 Device Recall Boston Scientific Scimed | 合法醫療器材資訊網
Premarket Approval (PMA) | 合法醫療器材資訊網
Scimed Life Systems Inc FDA Filings | 合法醫療器材資訊網
US4838269A | 合法醫療器材資訊網
必利勁怎麽服用達到治療效果 | 合法醫療器材資訊網
經皮穿刺末稍血管整形導管"SCIMED" PTA CATHETER ... | 合法醫療器材資訊網
經皮穿刺末稍血管整形導管"SCIMED" PTA CATHETER} | 合法醫療器材資訊網
經皮穿刺末稍血管整形導管"SCIMED" PTA CATHETER} | 合法醫療器材資訊網
相關資訊整理
【經皮穿刺末稍血管整形導管】許可證字號:衛署醫器輸字第007357號
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