Home GUDID 03760177046320 OSTEOFLEX
Primary DI 03760177046320
Brand OSTEOFLEX
Company TEKNIMED
Model VCF-1009
Catalog number VCF-1009
Published 2020-09-25
Public version status New
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 NDN Cement, Bone, Vertebroplasty
Product Code Classifications# Code, Device, Specialty table Code Device Specialty Class NDN Cement, Bone, Vertebroplasty Orthopedic 2
Identifiers And Packaging# Identifier, Type, Agency table Identifier Type Agency Package quantity Status 03760177046320 Primary GS1 0
Alternate GTIN / UPC / EAN Codes Source identifier, GTIN-14 normalized, EAN-13 table Source identifier GTIN-14 normalized EAN-13 03760177046320 03760177046320 3760177046320
GMDN Terms# Term, Definition table Term Definition Vertebral bone filler, non-bioabsorbable A sterile substance intended to be used to replace cortical/cancellous bone in a vertebral body to stabilize vertebral compression fractures (VCFs) caused by cancer, osteoporosis, or trauma. The device may be a sterile powder of a synthetic polymer [e.g., polymethylmethacrylate (PMMA)] that is mixed with its sterile diluent, or a non-PMMA-containing elastomer formed by mixing two precursors, prior to implantation typically during a balloon kyphoplasty or vertebroplasty procedure. This device does not contain an antibiotic agent. After application, this device cannot be reused.
Storage And Handling# Type, Low, High table Type Low High Condition Storage Environment Temperature 0 Degrees Celsius 25 Degrees Celsius
Regulatory Flags# DUNS number 764746723 Device count 1 DM exempt false Premarket exempt false HCT/P false Kit false Combination product false Lot or batch true Serial number true 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# Other Devices Sharing Product Codes# Primary DI, Brand, Company table Primary DI Brand Company Product code Published 08800038029323 SteriSpine VA IMEDICOM CO., LTD. NDN 2025-09-24 08800038029330 SteriSpine VA IMEDICOM CO., LTD. NDN 2025-09-24 08800038029347 SteriSpine VA IMEDICOM CO., LTD. NDN 2025-09-24 08800038029354 SteriSpine VA IMEDICOM CO., LTD. NDN 2025-09-24 08800038029361 SteriSpine VA IMEDICOM CO., LTD. NDN 2025-09-24 08800038029378 SteriSpine VA IMEDICOM CO., LTD. NDN 2025-09-24 08800038029415 SteriSpine VA IMEDICOM CO., LTD. NDN 2025-09-24 08800038029422 SteriSpine VA IMEDICOM CO., LTD. NDN 2025-09-24 08800038039407 SteriSpine VA IMEDICOM CO., LTD. NDN 2025-09-24 08800038039414 SteriSpine VA IMEDICOM CO., LTD. NDN 2025-09-24 08800038039421 SteriSpine VA IMEDICOM CO., LTD. NDN 2025-09-24 08800038039438 SteriSpine VA IMEDICOM CO., LTD. NDN 2025-09-24 08800038039445 SteriSpine VA IMEDICOM CO., LTD. NDN 2025-09-24 08800038039452 SteriSpine VA IMEDICOM CO., LTD. NDN 2025-09-24 08800038039469 SteriSpine VA IMEDICOM CO., LTD. NDN 2025-09-24 08800038039476 SteriSpine VA IMEDICOM CO., LTD. NDN 2025-09-24 08058964726452 Winch Kyphoplasty Kit 15 mm G21 SRL NDN 2025-02-26 08058964726469 Winch Kyphoplasty Kit 20 mm G21 SRL NDN 2025-02-26 08058964726735 Winch Kyphoplasty Bilateral Kit 15 mm G21 SRL NDN 2025-02-26 08058964727589 EasyWinch 15 mm G21 SRL NDN 2025-02-26 08058964727596 EasyWinch 20 mm G21 SRL NDN 2025-02-26 08058964727763 Winch Kyphoplasty Kit 8G 15 mm G21 SRL NDN 2025-02-26 08058964727770 Winch Kyphoplasty Bilateral Kit 8G 15 mm G21 SRL NDN 2025-02-26 08058964727787 Winch Kyphoplasty Kit 8G 20 mm G21 SRL NDN 2025-02-26 08058964727794 Winch Kyphoplasty Bilateral Kit 8G 20 mm G21 SRL NDN 2025-02-26 08058964727817 Winch Kyphoplasty Bilateral Kit 20 mm G21 SRL NDN 2025-02-26 07613327545258 AutoPlex VertaPlex STRYKER CORPORATION NDN 2024-11-21 07613327638226 Omnicurve STRYKER CORPORATION NDN 2024-09-03 07613327638233 Omnicurve STRYKER CORPORATION NDN 2024-09-03 07613327638240 Omnicurve STRYKER CORPORATION NDN 2024-09-03