Cruxi research & evidence
Biocompatibility Testing (ISO 10993 Program) evidence guides — page 24
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- OrthoPulse (K143120): indications, design and recorded evidenceRegulatory decision evidence
- OrthoPulse 2.0E (OPi2E-100) (K230905): indications, design and recorded evidenceRegulatory decision evidence
- OsteoMed PINNACLE Driver (K162542): indications, design and recorded evidenceRegulatory decision evidence
- OtoNova/OtoNova Pro (K234095): indications, design and recorded evidenceRegulatory decision evidence
- Otsuka Digital Feedback Device-RW (K223463): indications, design and recorded evidenceRegulatory decision evidence
- Owgels Oxygen Concentrator (K191875): indications, design and recorded evidenceRegulatory decision evidence
- Oxevision Sleep Device (K233618): indications, design and recorded evidenceRegulatory decision evidence
- P200DTx (K142897): indications, design and recorded evidenceRegulatory decision evidence
- P200MAAF (K102492): indications, design and recorded evidenceRegulatory decision evidence
- P300 Attachment (K202120): indications, design and recorded evidenceRegulatory decision evidence
- PALACOS R pro, PALACOS R+G pro, PALACOS MV+G pro (K210607): indications, design and recorded evidenceRegulatory decision evidence
- PASS LP Spinal System (K142798): indications, design and recorded evidenceRegulatory decision evidence
- PATHASSIST LED LIGHT FIBER (K141916): indications, design and recorded evidenceRegulatory decision evidence
- PATHASSIST LIGHT FIBER (K120962): indications, design and recorded evidenceRegulatory decision evidence
- PATHASSIT LIGHT SEEKER (K120735): indications, design and recorded evidenceRegulatory decision evidence
- PC ECG (K160876): indications, design and recorded evidenceRegulatory decision evidence
- PC ECG (K161302): indications, design and recorded evidenceRegulatory decision evidence
- PENTAX Medical Video Upper GI Scopes (EG Family), PENTAX Medical Video Colonoscopes (EC Family) (K210485): indications, design and recorded evidenceRegulatory decision evidence
- PENTAX Video Colonoscopes (EC Family) (K181084): indications, design and recorded evidenceRegulatory decision evidence
- PERIO-FLOW nozzle (K171174): indications, design and recorded evidenceRegulatory decision evidence
- PHILIPS AVALON FETAL / MATERNAL MONITORS FM20, FM30, FM40 AND FM50 (K140535): indications, design and recorded evidenceRegulatory decision evidence
- PICOCLAMP (K230281): indications, design and recorded evidenceRegulatory decision evidence
- POSEIDON ST (K261031): indications, design and recorded evidenceRegulatory decision evidence
- PTG-05 (K240347): indications, design and recorded evidenceRegulatory decision evidence
- PacePro Wire (K240864): indications, design and recorded evidenceRegulatory decision evidence
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