Medical Device Recalls | 合法醫療器材資訊網
Results401-500of500—TridentPSLHASolidBack50mmIncludesDomeHolePlugRef540-11-50EIntendedforcementless...63,2,02/03/2015,Stryker ...
References
R3 TM CERAMIC ACETABULAR LINER,
BIOLOX® FORTE, 36 MM O.D. 52 MM O.D., REF 71338952, STERILE
R, Q... (www.accessdata.fda.gov)
R3 TM CERAMIC ACETABULAR LINER,
BIOLOX® FORTE, 36 MM O.D. 54 MM O.D., REF 71338954, STERILE
R, Q... (www.accessdata.fda.gov)
R3 TM CERAMIC ACETABULAR LINER,
BIOLOX® FORTE, 36 MM O.D. 62 MM O.D., REF 71338962, STERILE
R, Q... (www.accessdata.fda.gov)
R3 TM CERAMIC ACETABULAR LINER,
BIOLOX® FORTE, 36 MM O.D. 56 MM O.D., REF 71338956, STERILE
R, Q... (www.accessdata.fda.gov)
R3 (TM) 28 MM I.D., 66/70 MM
O.D., CONSTRAINED LINER, UHMWPE, CO-CR, TI-6AL-4V, REF
71339166, STERIL...
(www.accessdata.fda.gov)
R3 (TM) 28 MM I.D., 64 MM O.D.,
CONSTRAINED LINER, UHMWPE, CO-CR, TI-6AL-4V, REF 71339164,
STERILE E...
stryker trident recall stryker trident recall 達勝資本 穿刺套管 conquest balloon Siemens chemistry analyzers "KARL STORZ" CONTACT-MICRO-COLPOHYSTEROSCOPE Dornier Compact Sigma 擺位椅 “AMO” IntraLase Patient Interface
Recalled Stryker Hip Implants | 合法醫療器材資訊網
Stryker Hip Lawsuit: Trident, ABG II | 合法醫療器材資訊網
The Trident Hemispherical Cup system and Trident Acetabular PSL Cup were both pulled off the market following a rash of adverse event reports and an FDA warning ... Read More
Medical Device Recalls | 合法醫療器材資訊網
Results 401 - 500 of 500 — Trident PSL HA Solid Back 50 mm Includes Dome Hole Plug Ref 540-11-50E Intended for cementless...63, 2, 02/03/2015, Stryker ... Read More
Class 2 Device Recall Stryker Trident Constrained Liner ... | 合法醫療器材資訊網
2016年7月25日 — Stryker notified its branches/agencies of this recall by e-mail on May 26, 2016. They were asked to quarantine the affected devices. Stryker ... Read More
Stryker Trident Recall | 合法醫療器材資訊網
2008年2月23日 — Last month, a Stryker Trident recall was issued for certain hip implant components. The recall came after months of production problems ... Read More
Stryker® Hip Recall | 合法醫療器材資訊網
Stryker® did not act until January 2008, when certain components of the Trident system were subject to a voluntary recall. The two components removed from the ... Read More
Stryker Hip Implant Recall | 合法醫療器材資訊網
Stryker also recalled hip implants in 2008 because of manufacturing issues. After receiving an FDA warning letter, the company stated that its Trident PSL ... Read More
Stryker Hip Replacement | 合法醫療器材資訊網
Mobile Bearing Hip System; Trident Acetabular Shell; Trident Alumina ... Stryker recalled two of its hip replacement systems that contained the alloy. Read More
Stryker Hip Implants Recall | 合法醫療器材資訊網
The Stryker hip implants that are defective and included in the recall are the Trident Acetabular PSL and the Trident Hemispherical Cups. Read More
相關資訊整理
【人工髖關節】許可證字號:衛署醫器輸字第009324號
器材品名:人工髖關節許可證字號:衛署醫器輸字第009324號註銷狀態:已註銷註銷日期:2007/08/28註銷理由:許可證已逾有效期有效...