Home GUDID 07640139342287 Dynamik Intervertebral Body Fusion Device
Primary DI 07640139342287
Brand Dynamik Intervertebral Body Fusion Device
Company SpineArt SA
Model DYN-BS 22 08-S
Catalog number DYN-BS 22 08-S
Device description Bone Substitute L22 H08
Published 2018-03-12
Public version status Update
Distribution status In Commercial Distribution
MRI safety Labeling does not contain MRI Safety Information
Rx true
OTC false
Sterile true
Single use true Product Codes# Code, Name table Code Name MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Product Code Classifications# Code, Device, Specialty table Code Device Specialty Class MAX Intervertebral Fusion Device With Bone Graft, Lumbar Orthopedic 2
Identifiers And Packaging# Identifier, Type, Agency table Identifier Type Agency Package quantity Status 07640139342287 Primary GS1 0
Alternate GTIN / UPC / EAN Codes Source identifier, GTIN-14 normalized, EAN-13 table Source identifier GTIN-14 normalized EAN-13 07640139342287 07640139342287 7640139342287
GMDN Terms# Term, Definition table Term Definition Orthopaedic bone void filling material, synthetic, bioabsorbable, non-antimicrobial A bioabsorbable, implantable device made of a synthetic material(s) intended to replace bone lost through trauma, surgery, or pathological conditions (e.g., osteoporosis); it is not dedicated to dental applications and does not include an antimicrobial agent(s). It may be made of ceramics (e.g., tricalcium phosphate or hydroxyapatite), bioactive glasses/minerals/metals (e.g., strontium), or bioabsorbable polymers. Also referred to as a graft, matrix, or void filler, it typically provides an osteoconductive scaffold that promotes bone growth, and is used to fill cystic defects, repair fractures, and/or extend autogenous bone grafts. It may have adhesive properties.
Device Sizes# Type, Value, Unit table Type Value Unit Height 0 Length 0
Storage And Handling# Type, Low, High table Type Low High Condition Storage Environment Temperature 0 0
Regulatory Flags# DUNS number 483016148 Device count 1 DM exempt false Premarket exempt false HCT/P false Kit false Combination product false Lot or batch true Serial number false Manufacturing date on label true Expiration date on label true Donation ID number false Contains natural rubber latex false No natural rubber latex false Sterilization required before use false Other Devices From This Company# Primary DI, Brand, Model table Primary DI Brand Model Catalog Published 07640139342294 Dynamik Intervertebral Body Fusion Device DYN-BS 22 10-S DYN-BS 22 10-S 2018-03-12 07640139342300 Dynamik Intervertebral Body Fusion Device DYN-BS 22 12-S DYN-BS 22 12-S 2018-03-12 07640139342317 Dynamik Intervertebral Body Fusion Device DYN-BS 22 14-S DYN-BS 22 14-S 2018-03-12 07640139343819 Dynamik Intervertebral Body Fusion Device DYN-BS 22 16-S DYN-BS 22 16-S 2018-03-12 07640151087500 BGran® Synthetic Osteoconductive Scaffold BGS-005 BGS-005 2017-09-18 07640151087517 BGran® Synthetic Osteoconductive Scaffold BGS-010 BGS-010 2017-09-18 07640151087524 BGran® Synthetic Osteoconductive Scaffold BGS-015 BGS-015 2017-09-18 07640151087531 BGran® Synthetic Osteoconductive Scaffold BGS-030 BGS-030 2017-09-18 07640151087654 BGran® Synthetic Osteoconductive Scaffold BGF-001 BGF-001 2017-09-18 07640151087661 BGran® Synthetic Osteoconductive Scaffold BGF-005 BGF-005 2017-09-18 07640151087678 BGran® Synthetic Osteoconductive Scaffold BGF-010 BGF-010 2017-09-18 07640151087685 BGran® Synthetic Osteoconductive Scaffold BGL-015 BGL-015 2017-09-18 07640151087692 BGran® Synthetic Osteoconductive Scaffold BGL-030 BGL-030 2017-09-18 07640139343185 BAGUERA C INSTRUMENTATION CDP-IN 30 01-N 2026-08-27 07640221370884 TRYPTIK® Ti TRY-BX 40 01-N 2026-08-27 07640178972452 ROMEO posterior osteosynthesis system NAV-IN 01 00-N NAV-IN 01 00-N 2019-01-31 07640221370891 BAGUERA® C BAG-CT 13 05-S 2026-08-21 07640221370907 BAGUERA® C BAG-CT 13 06-S 2026-08-21 07640221370914 BAGUERA® C BAG-CT 13 07-S 2026-08-21 07640221370921 BAGUERA® C BAG-CT 14 05-S 2026-08-21
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