Home GUDID H98104102045S0
ANTEGRA-T
Primary DI H98104102045S0
Brand ANTEGRA-T
Company Synthes GmbH
Model 04.102.045S
Catalog number 04102045S
Device description TI ANTEGRA-T PLATE-STERILE 45MM-42MM LENGTH-LUMBAR
Published 2015-09-14
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 KWQ APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY
Product Code Classifications# Code, Device, Specialty table Code Device Specialty Class KWQ Appliance, Fixation, Spinal Intervertebral Body Orthopedic 2
Identifiers And Packaging# Identifier, Type, Agency table Identifier Type Agency Package quantity Status 10705034732930 Primary GS1 0 H98104102045S0 Secondary HIBCC 0
Alternate GTIN / UPC / EAN Codes Source identifier, GTIN-14 normalized table Source identifier GTIN-14 normalized 10705034732930 10705034732930
GMDN Terms# Term, Definition table Term Definition Bone-screw internal spinal fixation system, sterile An assembly of 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. Sterile disposable devices associated with implantation may be included.
Regulatory Flags# DUNS number 486711679 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 false 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# Other Devices Sharing Product Codes# Primary DI, Brand, Company table Primary DI Brand Company Product code Published 00840466901035 Primus SPINAL ELEMENTS, INC. KWQ 2026-07-21 00840466901042 Primus SPINAL ELEMENTS, INC. KWQ 2026-07-21 00840466901059 Primus SPINAL ELEMENTS, INC. KWQ 2026-07-21 00840466901066 Primus SPINAL ELEMENTS, INC. KWQ 2026-07-21 00840466901073 Primus SPINAL ELEMENTS, INC. KWQ 2026-07-21 00840466901080 Primus SPINAL ELEMENTS, INC. KWQ 2026-07-21 00840466901097 Primus SPINAL ELEMENTS, INC. KWQ 2026-07-21 00840466901103 Primus SPINAL ELEMENTS, INC. KWQ 2026-07-21 00840466901110 Primus SPINAL ELEMENTS, INC. KWQ 2026-07-21 00840466901127 Primus SPINAL ELEMENTS, INC. KWQ 2026-07-21 00840466901141 Primus SPINAL ELEMENTS, INC. KWQ 2026-07-21 00840466901158 Primus SPINAL ELEMENTS, INC. KWQ 2026-07-21 00840466901165 Primus SPINAL ELEMENTS, INC. KWQ 2026-07-21 00840466901172 Primus SPINAL ELEMENTS, INC. KWQ 2026-07-21 00840466901479 Primus SPINAL ELEMENTS, INC. KWQ 2026-07-21 00840466901486 Primus SPINAL ELEMENTS, INC. KWQ 2026-07-21 00840466901493 Primus SPINAL ELEMENTS, INC. KWQ 2026-07-21 00840466901509 Primus SPINAL ELEMENTS, INC. KWQ 2026-07-21 00840466901516 Primus SPINAL ELEMENTS, INC. KWQ 2026-07-21 00840466901523 Primus SPINAL ELEMENTS, INC. KWQ 2026-07-21 00840466901530 Primus SPINAL ELEMENTS, INC. KWQ 2026-07-21 00840466901547 Primus SPINAL ELEMENTS, INC. KWQ 2026-07-21 00840466901554 Primus SPINAL ELEMENTS, INC. KWQ 2026-07-21 00840466901561 Primus SPINAL ELEMENTS, INC. KWQ 2026-07-21 00840466901578 Primus SPINAL ELEMENTS, INC. KWQ 2026-07-21 00840466901585 Primus SPINAL ELEMENTS, INC. KWQ 2026-07-21 00840466901592 Primus SPINAL ELEMENTS, INC. KWQ 2026-07-21 00840466901608 Primus SPINAL ELEMENTS, INC. KWQ 2026-07-21 00840466901615 Primus SPINAL ELEMENTS, INC. KWQ 2026-07-21 00840466901622 Primus SPINAL ELEMENTS, INC. KWQ 2026-07-21