Cruxi research & evidence
Biocompatibility Testing (ISO 10993 Program) evidence guides — page 2
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- ALBAAD PLASTIC APPLICATOR TAMPONS UNSCENTED (K140077): indications, design and recorded evidenceRegulatory decision evidence
- ALGO Pro Newborn Hearing Screener (ALGO Pro) (K233649): indications, design and recorded evidenceRegulatory decision evidence
- ALYTE Y-MESH GRAFT (K101722): indications, design and recorded evidenceRegulatory decision evidence
- AMBARINO High-Class (K222723): indications, design and recorded evidenceRegulatory decision evidence
- AMERIWATER CENTURION 1500+ REVERSE OSMOSIS SYSTEM WITH HEAT SANITIZATION (K133783): indications, design and recorded evidenceRegulatory decision evidence
- AMIGO REMOTE CATHETER SYSTEM & ACCESSORIES (K122488): indications, design and recorded evidenceRegulatory decision evidence
- AMSure Hydrophilic Intermittent Catheter (K181445): indications, design and recorded evidenceRegulatory decision evidence
- AMT G-Tube Balloon Gastrostomy Feeding Device (K222846): indications, design and recorded evidenceRegulatory decision evidence
- AMT Suture Delivery System (K193612): indications, design and recorded evidenceRegulatory decision evidence
- ANNE Chest (K240251): indications, design and recorded evidenceRegulatory decision evidence
- ANNE One (K223711): indications, design and recorded evidenceRegulatory decision evidence
- AOI CRANIAL HELMET (K103362): indications, design and recorded evidenceRegulatory decision evidence
- APRO 55 Catheter (K234115): indications, design and recorded evidenceRegulatory decision evidence
- AQUAbase nX (K223479): indications, design and recorded evidenceRegulatory decision evidence
- ASTM E1262-24 — FDA recognition transition and report handoffCompliance research
- ASTM F1439-24 — FDA recognition transition and report handoffCompliance research
- ASTM F1877-24 — FDA recognition transition and report handoffCompliance research
- ASTM F1984-25 — FDA recognition transition and report handoffCompliance research
- ASTM F2382-24 — FDA recognition transition and report handoffCompliance research
- ASTM F720-24 — FDA recognition transition and report handoffCompliance research
- ASTM F748-25 — FDA recognition transition and report handoffCompliance research
- ASTM F895-25 — FDA recognition transition and report handoffCompliance research
- AT 030 (K180839): indications, design and recorded evidenceRegulatory decision evidence
- AVACEN 100 (K133981): indications, design and recorded evidenceRegulatory decision evidence
- AXIOS Stent and Delivery System, AXIOS Stent and Electrocautery Enhanced Delivery System (K181905): indications, design and recorded evidenceRegulatory decision evidence
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