Cruxi research & evidence
Biocompatibility Testing (ISO 10993 Program) evidence guides — page 29
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- Reprocessed LigaSure ImpactTM Curved, Large Jaw, Open Sealer/Divider (K150538): indications, design and recorded evidenceRegulatory decision evidence
- Reprocessed ViewFlex Xtra ICE Catheter (K182238): indications, design and recorded evidenceRegulatory decision evidence
- Resection Electrodes (K152092): indications, design and recorded evidenceRegulatory decision evidence
- Resona A10S, Resona A20 Pro, Resona A20T, Resona A20S, Resona A20W, Resona A20, Resona A20 Exp, Resona A20 Premium, Resona A20 Elite, Resona A20 Plus, Resona A Elite, Resona A MV, Eagus A20W, Eagus A20 Diagnostic Ultrasound System (K253049): indications, design and recorded evidenceRegulatory decision evidence
- Restoration Modular 115mm Conical Distal Stem (K213129): indications, design and recorded evidenceRegulatory decision evidence
- RetroPerc Flexible Ureteroscopy-Guided Retrograde Nephrostomy Wire Puncture Set (K160077): indications, design and recorded evidenceRegulatory decision evidence
- Reusable and Self-Adhesive Electrodes (K180773): indications, design and recorded evidenceRegulatory decision evidence
- Rochal Bioshield Silicone Film (K182733): indications, design and recorded evidenceRegulatory decision evidence
- Route 92 Medical 088 Access System (K201518): indications, design and recorded evidenceRegulatory decision evidence
- Route 92 Medical Full Length 070 Reperfusion System and Aspiration Tubing Set (K223530): indications, design and recorded evidenceRegulatory decision evidence
- Rx Knee System (K240683): indications, design and recorded evidenceRegulatory decision evidence
- SB Soft Hood - Straight type, SB Soft Hood - Undercut type (K173004): indications, design and recorded evidenceRegulatory decision evidence
- SENSATION PLUS 7.5FR. 40CC INTRA-AORTIC BALLOON (IAB) CATHETER AND ACCESSORIES (K122628): indications, design and recorded evidenceRegulatory decision evidence
- SI-LOK® Sacroiliac Joint Fixation System, Navigation Instruments, ExcelsiusGPS® Instruments (K183119): indications, design and recorded evidenceRegulatory decision evidence
- SIDDHARTH-II; IMPACT (K210894): indications, design and recorded evidenceRegulatory decision evidence
- SIGMA Sterilization Pouch and Roll (K202462): indications, design and recorded evidenceRegulatory decision evidence
- SILK Surgical Suture (K162396): indications, design and recorded evidenceRegulatory decision evidence
- SINUSPRIME Dilation System (K201398): indications, design and recorded evidenceRegulatory decision evidence
- SIRIUS Endoscope System (K221642): indications, design and recorded evidenceRegulatory decision evidence
- SONOSURE SONOHYSTEROGRAPHY & ENDOMETRIAL SAMPLING DEVICE (K133144): indications, design and recorded evidenceRegulatory decision evidence
- SP Endoscope, 0° (430600) (K250786): indications, design and recorded evidenceRegulatory decision evidence
- SPECULUM, VAGINAL, NONMETAL (K120743): indications, design and recorded evidenceRegulatory decision evidence
- STIMPOD NMS460 Nerve Stimulator (K252712): indications, design and recorded evidenceRegulatory decision evidence
- STRYKER CMF MEDPOR CUSTOMIZED IMPLANT (K121315): indications, design and recorded evidenceRegulatory decision evidence
- STRYKER INFRARED ILLUMINATION SYSTEM (IRIS) [AIM Light Source and IRIS Ureteral Kit] (K151243): indications, design and recorded evidenceRegulatory decision evidence
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