Home GUDID 00841523106899
Kyocera Medical Technologies, Inc.
Primary DI 00841523106899
Brand Kyocera Medical Technologies, Inc.
Company KYOCERA MEDICAL TECHNOLOGIES, INC.
Model S 100
Catalog number 1101-053-045
Device description Pre Lordosed Rod 5.5mm diameter 45mm length Ti6Al4V
Published 2015-10-29
Public version status Update
Distribution status In Commercial Distribution
MRI safety Labeling does not contain MRI Safety Information
Rx true
Single use true Product Codes# Code, Name table Code Name KWP Appliance, Fixation, Spinal Interlaminal MNH Orthosis, Spondylolisthesis Spinal Fixation MNI Orthosis, Spinal Pedicle Fixation
Product Code Classifications# Code, Device, Specialty table Code Device Specialty Class KWP Appliance, Fixation, Spinal Interlaminal Orthopedic 2 MNH Orthosis, Spondylolisthesis Spinal Fixation Orthopedic 2 MNI Orthosis, Spinal Pedicle Fixation Orthopedic 2
Identifiers And Packaging# Identifier, Type, Agency table Identifier Type Agency Package quantity Status 00841523106899 Primary GS1 0
Alternate GTIN / UPC / EAN Codes Source identifier, GTIN-14 normalized, UPC-A table Source identifier GTIN-14 normalized UPC-A EAN-13 00841523106899 00841523106899 841523106899 0841523106899
GMDN Terms# Term, Definition table Term Definition Bone-screw internal spinal fixation system, non-sterile An assembly of non-sterile implantable devices intended to provide immobilization and stabilization of spinal segments in the treatment of various spinal instabilities or deformities, also used as an adjunct to spinal fusion [e.g., for degenerative disc disease (DDD)]. Otherwise known as a pedicle screw instrumentation system, it typically consists of a combination of anchors (e.g., bolts, hooks, pedicle screws or other types), interconnection mechanisms (incorporating nuts, screws, sleeves, or bolts), longitudinal members (e.g., plates, rods, plate/rod combinations), and/or transverse connectors. Non-sterile disposable devices associated with implantation may be included.
Sterilization Methods# Method table Method Moist Heat or Steam Sterilization
Regulatory Flags# DUNS number 116995646 Device count 1 Lot or batch true Sterilization required before use true Other Devices From This Company# Primary DI, Brand, Model table Primary DI Brand Model Catalog Published 00841523146871 Kyocera Medical Technologies, Inc. S 180 3180-004-001 2025-04-08 00841523146888 Kyocera Medical Technologies, Inc. S 180 3180-004-002 2025-04-08 00841523146901 Kyocera Medical Technologies, Inc. S 180 3180-005-001 2025-04-08 00841523146918 Kyocera Medical Technologies, Inc. S 180 3180-005-002 2025-04-08 00841523146932 Kyocera Medical Technologies, Inc. S 180 3180-006-000 2025-04-08 00841523146949 Kyocera Medical Technologies, Inc. S 180 3180-006-001 2025-04-08 00841523146956 Kyocera Medical Technologies, Inc. S 180 3180-007-000 2025-04-08 00841523137060 Kyocera Medical Technologies, Inc. S 128 1063-730-617 2019-01-17 00841523181360 Kyocera Medical Technologies, Inc. Tesera-k PL 2171-001-001 2026-05-26 00841523181681 Kyocera Medical Technologies, Inc. Tesera-k PL 2171-221-107 2026-05-26 00841523181698 Kyocera Medical Technologies, Inc. Tesera-k PL 2171-221-108 2026-05-26 00841523181704 Kyocera Medical Technologies, Inc. Tesera-k PL 2171-221-109 2026-05-26 00841523181711 Kyocera Medical Technologies, Inc. Tesera-k PL 2171-221-110 2026-05-26 00841523181728 Kyocera Medical Technologies, Inc. Tesera-k PL 2171-221-111 2026-05-26 00841523181735 Kyocera Medical Technologies, Inc. Tesera-k PL 2171-221-112 2026-05-26 00841523181742 Kyocera Medical Technologies, Inc. Tesera-k PL 2171-221-113 2026-05-26 00841523181759 Kyocera Medical Technologies, Inc. Tesera-k PL 2171-221-114 2026-05-26 00841523181766 Kyocera Medical Technologies, Inc. Tesera-k PL 2171-221-115 2026-05-26 00841523181773 Kyocera Medical Technologies, Inc. Tesera-k PL 2171-221-116 2026-05-26 00841523181780 Kyocera Medical Technologies, Inc. Tesera-k PL 2171-229-107 2026-05-26
Other Devices Sharing Product Codes# Primary DI, Brand, Company table Primary DI Brand Company Product code Published B678520297S0 PressON™ NEXUS SPINE, L.L.C. MNI 2026-07-10 B678520297S0 PressON™ NEXUS SPINE, L.L.C. MNH 2026-07-10 B678520298S0 PressON™ NEXUS SPINE, L.L.C. MNH 2026-07-10 B678520298S0 PressON™ NEXUS SPINE, L.L.C. MNI 2026-07-10 B678520299S0 PressON NEXUS SPINE, L.L.C. MNH 2026-07-10 B678520299S0 PressON NEXUS SPINE, L.L.C. MNI 2026-07-10 B678520300S0 PressON™ NEXUS SPINE, L.L.C. MNH 2026-07-10 B678520300S0 PressON™ NEXUS SPINE, L.L.C. MNI 2026-07-10 B678520301S0 PressON NEXUS SPINE, L.L.C. MNH 2026-07-10 B678520301S0 PressON NEXUS SPINE, L.L.C. MNI 2026-07-10 B678520302S0 PressON™ NEXUS SPINE, L.L.C. MNH 2026-07-10 B678520302S0 PressON™ NEXUS SPINE, L.L.C. MNI 2026-07-10 B678520303S0 PressON NEXUS SPINE, L.L.C. MNH 2026-07-10 B678520303S0 PressON NEXUS SPINE, L.L.C. MNI 2026-07-10 B678520304S0 PressON™ NEXUS SPINE, L.L.C. MNI 2026-07-10 B678520304S0 PressON™ NEXUS SPINE, L.L.C. MNH 2026-07-10 B678520305S0 PressON NEXUS SPINE, L.L.C. MNH 2026-07-10 B678520305S0 PressON NEXUS SPINE, L.L.C. MNI 2026-07-10 B678520306S0 PressON™ NEXUS SPINE, L.L.C. MNH 2026-07-10 B678520306S0 PressON™ NEXUS SPINE, L.L.C. MNI 2026-07-10 00643169465879 MSB CD HORIZON Spinal System MEDTRONIC SOFAMOR DANEK, INC. MNH 2026-06-28 00643169465879 MSB CD HORIZON Spinal System MEDTRONIC SOFAMOR DANEK, INC. KWP 2026-06-28 00643169465879 MSB CD HORIZON Spinal System MEDTRONIC SOFAMOR DANEK, INC. MNI 2026-06-28 00643169101296 MSB VERTEX® Reconstruction System MEDTRONIC SOFAMOR DANEK, INC. KWP 2026-06-27 10889981441555 VIRATA Seaspine Orthopedics Corporation KWP 2026-06-24 10889981441609 VIRATA Seaspine Orthopedics Corporation KWP 2026-06-24 10889981441616 VIRATA Seaspine Orthopedics Corporation KWP 2026-06-24 10889981441623 VIRATA Seaspine Orthopedics Corporation KWP 2026-06-24 10889981441661 VIRATA Seaspine Orthopedics Corporation KWP 2026-06-24 10889981005115 Newport Seaspine Orthopedics Corporation MNH 2015-09-24