Home GUDID 00841379162964 BRIDALVEIL
Primary DI 00841379162964
Brand BRIDALVEIL
Company Astura Medical
Model FFBA00R80
Catalog number FFBA00R80
Device description RIGHT OFFSET HOOK
Published 2021-07-23
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 NKG Posterior Cervical Screw System
Product Code Classifications# Code, Device, Specialty table Code Device Specialty Class KWP Appliance, Fixation, Spinal Interlaminal Orthopedic 2 NKG Posterior Cervical Screw System Orthopedic 2
Identifiers And Packaging# Identifier, Type, Agency table Identifier Type Agency Package quantity Status 00841379162964 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 00841379162964 00841379162964 841379162964 0841379162964
GMDN Terms# Term, Definition table Term Definition Bone-screw internal spinal fixation system hook An implantable component of a bone-screw internal spinal fixation system that has a curved (hook-shaped) design intended to provide immobilization and stabilization of spinal segments in the treatment of various spinal instabilities or deformities, and also used as an adjunct to spinal fusion [e.g., for degenerative disc disease (DDD)]. This component is typically made of metal [e.g., titanium (Ti)] and placed/hooked around the lamina or pedicle of a vertebra, without penetration (i.e., not a screw), to provide a stable connection for the system’s rod; the rod is typically stabilized in the U-shaped hook head with a small lid or screw.
Device Sizes# Type, Value, Unit table Type Value Unit Outer Diameter 8 Millimeter
Sterilization Methods# Method table Method Moist Heat or Steam Sterilization
Regulatory Flags# DUNS number 073029645 Device count 1 Lot or batch true Sterilization required before use true Other Devices From This Company# Other Devices Sharing Product Codes# Primary DI, Brand, Company table Primary DI Brand Company Product code Published 00840466901011 Primus SPINAL ELEMENTS, INC. KWP 2026-10-22 00840019978156 Reform Ti PRECISION SPINE, INC. KWP 2026-10-19 00840019978163 Reform Ti PRECISION SPINE, INC. KWP 2026-10-19 00840019978170 Reform Ti PRECISION SPINE, INC. KWP 2026-10-19 00840019978187 Reform Ti PRECISION SPINE, INC. KWP 2026-10-19 00840019978194 Reform Ti PRECISION SPINE, INC. KWP 2026-10-19 00840019978200 Reform Ti PRECISION SPINE, INC. KWP 2026-10-19 00840019978217 Reform Ti PRECISION SPINE, INC. KWP 2026-10-19 00840019978224 Reform Ti PRECISION SPINE, INC. KWP 2026-10-19 00840019978231 Reform Ti PRECISION SPINE, INC. KWP 2026-10-19 00840019978248 Reform Ti PRECISION SPINE, INC. KWP 2026-10-19 00840019978255 Reform Ti PRECISION SPINE, INC. KWP 2026-10-19 00840019978262 Reform Ti PRECISION SPINE, INC. KWP 2026-10-19 00840019978279 Reform Ti PRECISION SPINE, INC. KWP 2026-10-19 00840019978286 Reform Ti PRECISION SPINE, INC. KWP 2026-10-19 00840019978293 Reform Ti PRECISION SPINE, INC. KWP 2026-10-19 00840019978309 Reform Ti PRECISION SPINE, INC. KWP 2026-10-19 00840019978316 Reform Ti PRECISION SPINE, INC. KWP 2026-10-19 00840019978323 Reform Ti PRECISION SPINE, INC. KWP 2026-10-19 00840019978330 Reform Ti PRECISION SPINE, INC. KWP 2026-10-19 00840019978347 Reform Ti PRECISION SPINE, INC. KWP 2026-10-19 00840019978354 Reform Ti PRECISION SPINE, INC. KWP 2026-10-19 00840019978361 Reform Ti PRECISION SPINE, INC. KWP 2026-10-19 00840019978378 Reform Ti PRECISION SPINE, INC. KWP 2026-10-19 00840019978385 Reform Ti PRECISION SPINE, INC. KWP 2026-10-19 00840019978392 Reform Ti PRECISION SPINE, INC. KWP 2026-10-19 00840019978408 Reform Ti PRECISION SPINE, INC. KWP 2026-10-19 00840019978415 Reform Ti PRECISION SPINE, INC. KWP 2026-10-19 00840019978422 Reform Ti PRECISION SPINE, INC. KWP 2026-10-19 00840019978439 Reform Ti PRECISION SPINE, INC. KWP 2026-10-19