Cruxi research & evidence
Biocompatibility Testing (ISO 10993 Program) evidence guides — page 35
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- URETRON MODEL URT (K111058): indications, design and recorded evidenceRegulatory decision evidence
- UbiqVue 2A Multi-parameter System (UX2550) (K242018): indications, design and recorded evidenceRegulatory decision evidence
- Ultra (samfilcon A) Multifocal for Astigmatism Contact Lens (K182249): indications, design and recorded evidenceRegulatory decision evidence
- UltraCor Twirl Breast Tissue Marker (K152510): indications, design and recorded evidenceRegulatory decision evidence
- UltraShape System (K162163): indications, design and recorded evidenceRegulatory decision evidence
- Ultrast Gel (K211691): indications, design and recorded evidenceRegulatory decision evidence
- Uni-FuZe-C Bone Strip (K221726): indications, design and recorded evidenceRegulatory decision evidence
- Uni-FuZe-P Bone Putty (K201781): indications, design and recorded evidenceRegulatory decision evidence
- UniVy OsteoVy Cervical IBF System (K221162): indications, design and recorded evidenceRegulatory decision evidence
- Universal Seal (5-12 mm) (K241360): indications, design and recorded evidenceRegulatory decision evidence
- Universal Seal (5-12 mm) (K253978): indications, design and recorded evidenceRegulatory decision evidence
- Upper Arm Electronic Blood Pressure Monitor (FC-BP107, FC-BP123, FC-BP125, FC-BP126, FC-BP127, FC-BP116) (K252769): indications, design and recorded evidenceRegulatory decision evidence
- Ureteral Dilator Sets, Ureteral Dilators (K173654): indications, design and recorded evidenceRegulatory decision evidence
- V12 PRO (K210913): indications, design and recorded evidenceRegulatory decision evidence
- V8/XV8/XH8/H8/cV8/V8 ONE/XV8 ONE/XH8 ONE/H8 ONE/cV8 ONE Diagnostic Ultrasound System; V7/XV7/XH7/H7/cV7/V7 ONE/XV7 ONE/H7 ONE/XH7 ONE/cV7 ONE Diagnostic Ultrasound System; V6/XV6/XH6/H6/cV6/V6 ONE/XV6 ONE/H6 ONE/XH6 ONE/cV6 ONE Diagnostic Ultrasound System; V5/XV5/XH5/H5/cV5 Diagnostic Ultrasound System; V4/XV4/XH4/H4/cV4 Diagnostic Ultrasound System; (K261412): indications, design and recorded evidenceRegulatory decision evidence
- VICTUS Femtosecond Laser Platform (K171014): indications, design and recorded evidenceRegulatory decision evidence
- VITA VIONIC Bond (K191926): indications, design and recorded evidenceRegulatory decision evidence
- VK100 Percutaneous Vertebral Augmentation System (K192403): indications, design and recorded evidenceRegulatory decision evidence
- VM-2000 (K240807): indications, design and recorded evidenceRegulatory decision evidence
- VORTRAN APM-Plus (K182292): indications, design and recorded evidenceRegulatory decision evidence
- VORTRAN GO2VENT with PEEP Valve (K202219): indications, design and recorded evidenceRegulatory decision evidence
- VS Newborn Heart Rate Monitor (K201887): indications, design and recorded evidenceRegulatory decision evidence
- VS3 Iridium Sytem (K210265): indications, design and recorded evidenceRegulatory decision evidence
- Vantage® Total Ankle System (K232002): indications, design and recorded evidenceRegulatory decision evidence
- VasQ (K240119): indications, design and recorded evidenceRegulatory decision evidence
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