Cruxi research & evidence
Biocompatibility Testing (ISO 10993 Program) evidence guides — page 4
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- Ascend VBR System, Ascend NanoTec VBR System (K232173): indications, design and recorded evidenceRegulatory decision evidence
- Aspiron(TM) Aspiration Catheter (K190619): indications, design and recorded evidenceRegulatory decision evidence
- AtriClip LAA Exclusion System with preloaded Gillinov-Cosgrove Clip (K150996): indications, design and recorded evidenceRegulatory decision evidence
- AtriClip LAA Exclusion System with preloaded Gillinov-Cosgrove Clip (K160454): indications, design and recorded evidenceRegulatory decision evidence
- AtriClip LAA Exclusion System with preloaded Gillinov-Cosgrove PRO V Clip (K153500): indications, design and recorded evidenceRegulatory decision evidence
- Automatic Tissue Processing Unit (K172717): indications, design and recorded evidenceRegulatory decision evidence
- Aveir Retrieval Catheter (K213494): indications, design and recorded evidenceRegulatory decision evidence
- Avitus® DragonWing Large Volume Autograft Delivery System (K231456): indications, design and recorded evidenceRegulatory decision evidence
- Axeo 3 Patient Monitor (K153079): indications, design and recorded evidenceRegulatory decision evidence
- BD AutoShield Duo Pen Needle (K223286): indications, design and recorded evidenceRegulatory decision evidence
- BD Nano 2nd Gen Pen Needle (K212015): indications, design and recorded evidenceRegulatory decision evidence
- BD Preset Syringe & BD A-Line Syringe (K202446): indications, design and recorded evidenceRegulatory decision evidence
- BENCOX Mirabo Cup System (K220468): indications, design and recorded evidenceRegulatory decision evidence
- BIOPHOTAS CELLUMA (K131113): indications, design and recorded evidenceRegulatory decision evidence
- BOVINE PERICARDIUM PATCH (K141721): indications, design and recorded evidenceRegulatory decision evidence
- BP Go (BPP-855) (K261061): indications, design and recorded evidenceRegulatory decision evidence
- BRELLA-SPEC(TM) VAGINAL SPECULUM (K133857): indications, design and recorded evidenceRegulatory decision evidence
- BUSSE EPIDURAL CATHETER KIT (K093920): indications, design and recorded evidenceRegulatory decision evidence
- Babyleo TN500 (K162821): indications, design and recorded evidenceRegulatory decision evidence
- Babyroo TN300 (K230278): indications, design and recorded evidenceRegulatory decision evidence
- Barrier Sleeves (K191448): indications, design and recorded evidenceRegulatory decision evidence
- Beacon EUS Access System (K180037): indications, design and recorded evidenceRegulatory decision evidence
- BeneVision N12, BeneVision N15, BeneVision N17, BeneVision N19, BeneVision N22, BeneVision N1 (K202405): indications, design and recorded evidenceRegulatory decision evidence
- Bicarby Dialysate RFP-402 (RFP-402-G); Bicarby Dialysate RFP-400 (RFP-400-G); Bicarby Dialysate RFP-407 (RFP-407-G); Bicarby Dialysate RFP-401 (RFP-401-G); Bicarby Dialysate RFP-404 (RFP-404-G); Bicarby Dialysate RFP-456 (RFP-456-G); Ci-Ca Dialysate 2K (RFP-457-G); Ci-Ca Dialysate 4K (RFP-458-G) (K243786): indications, design and recorded evidenceRegulatory decision evidence
- Bindex BI-100 (K152020): indications, design and recorded evidenceRegulatory decision evidence
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