MENDEC AQUA CARTRIDGE

GUDID 28031497002006

Mendec Aqua Cartridge is intended to be used with Mendec Aqua in vertebral augmentation procedure (vertebroplasty, kyphoplasty and screw-augmentation) when the acrylic resin/bone void filler loaded in a single cartridge is not sufficient to complete the surgical procedure.

TECRES SPA

Orthopaedic cement preparation/delivery kit
Primary Device ID28031497002006
NIH Device Record Keyfe261c78-667a-4232-96c6-1e8b269b8efc
Commercial Distribution StatusIn Commercial Distribution
Brand NameMENDEC AQUA CARTRIDGE
Version Model NumberASC0030
Company DUNS435428396
Company NameTECRES SPA
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS128031497002006 [Primary]

FDA Product Code

OARInjector, Vertebroplasty (Does Not Contain Cement)

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2022-10-03
Device Publish Date2022-09-23

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08031497003931 - InterSpace Hip Trial, 54mm Long2026-02-19
08031497003948 - InterSpace Hip Trial, 60mm Long2026-02-19
08031497003955 - Interspace GV Hip Spacer 462026-02-19 TAPERED WEDGE STEM
08031497003962 - Interspace GV Hip Spacer 542026-02-19 TAPERED WEDGE STEM

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