Cruxi research & evidence
Biocompatibility Testing (ISO 10993 Program) evidence guides — page 25
Compare documented facts, dated analyses and evidence that can change your project scope. Confirm applicability with a specialist.
Compare Biocompatibility Testing (ISO 10993 Program) providers- Painless IPL System - KDT750 (K220214): indications, design and recorded evidenceRegulatory decision evidence
- Pathfinder Endoscope Overtube (K191415): indications, design and recorded evidenceRegulatory decision evidence
- Patient Monitor, models LMPLUS-12, LMPLUS-15 and LMPLUS-17 (K221616): indications, design and recorded evidenceRegulatory decision evidence
- PeDIA (K181424): indications, design and recorded evidenceRegulatory decision evidence
- Peak Left Ventricular Vent Cannula, 20 Fr.; Peak Left Ventricular Vent Cannula, 18 Fr; Peak Left Ventricular Vent Cannula, 16 Fr (K170488): indications, design and recorded evidenceRegulatory decision evidence
- Pediatric Nailing Platform Tibia (K231266): indications, design and recorded evidenceRegulatory decision evidence
- Pediatric Nailing Platform Tibia Pediatric Nailing Platform Femur (K250623): indications, design and recorded evidenceRegulatory decision evidence
- Peel-Away Introducer (405104, 405108, 405112, 405116, 405118, 405119, 405120, 405122, 405124, 405128, 405129, 405136, 405144, 405145, 405146, 405147, 405149, 405153, 405154, 405254, 405269, 405270, 405404, 405408, 405412, 405416, 405418, 405420, 405422, 405424, 405428) (K230283): indications, design and recorded evidenceRegulatory decision evidence
- Penumbra 3D Revascularization Device (K162901): indications, design and recorded evidenceRegulatory decision evidence
- Penumbra System (Reperfusion Catheter RED 62) (K203440): indications, design and recorded evidenceRegulatory decision evidence
- Penumbra System (Reperfusion Catheter RED 72) (K211654): indications, design and recorded evidenceRegulatory decision evidence
- Penumbra System (Reperfusion Catheter RED 72) (K242104): indications, design and recorded evidenceRegulatory decision evidence
- Penumbra System 110 Aspiration Tubing (K151623): indications, design and recorded evidenceRegulatory decision evidence
- Pepper EMS Training System (K233770): indications, design and recorded evidenceRegulatory decision evidence
- Peregrine Endoscopy System (K202727): indications, design and recorded evidenceRegulatory decision evidence
- Perfect-O Ostial Positioning Catheter (K260289): indications, design and recorded evidenceRegulatory decision evidence
- Permatage Settable Bone Putty (K241027): indications, design and recorded evidenceRegulatory decision evidence
- Personal Kinetigraph (PKG) System (K161717): indications, design and recorded evidenceRegulatory decision evidence
- Phasix Mesh (K142818): indications, design and recorded evidenceRegulatory decision evidence
- Phasix ST Mesh (K143380): indications, design and recorded evidenceRegulatory decision evidence
- Philips Reusable ECG Lead Sets and Trunk Cables : Model Number,Model Name: 989803170171, OR 3-Lead ECG Trunk Cable, AAMI/IEC; 989803170181, OR 5-Lead ECG Trunk Cable, AAMI/IEC; M1667A, 6 Lead ECG Trunk, AAMI/IEC 2.7m; M1668A,5 Lead ECG Trunk, AAMI/IEC 2.7m; M1669A,3 Lead ECG Trunk, AAMI/IEC 2.7m; M1949A,5+5 ECG Trunk cable AAMI, IEC 2.7m; M1663A,10 Lead ECG Trunk AAMI/IEC 2m; M1665A, 6+4 Lead ECG Trunk AAMI/IEC 2.7m; M1671A, 3 Leadset, Grabber, AAMI, ICU; M1673A, 3 Leadset, Sn (K243545): indications, design and recorded evidenceRegulatory decision evidence
- Philips wearable biosensor-G5 Solution (K181165): indications, design and recorded evidenceRegulatory decision evidence
- PhotoFix Decellularized Bovine Pericardium (K162506): indications, design and recorded evidenceRegulatory decision evidence
- PhotonBlade 3; PhotonBlade 3 Smoke Evacuation (K250483): indications, design and recorded evidenceRegulatory decision evidence
- Piccolo Medical SmartPICC System (K200037): indications, design and recorded evidenceRegulatory decision evidence
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