MectaCem BonePrep

GUDID 08031497002842

TECRES SPA

Orthopaedic cement preparation/delivery kit
Primary Device ID08031497002842
NIH Device Record Keye370f17c-4e9a-4468-b22a-d3fe7e61133e
Commercial Distribution StatusIn Commercial Distribution
Brand NameMectaCem BonePrep
Version Model Number20.00003
Company DUNS435428396
Company NameTECRES SPA
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
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
GS108031497002842 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

JDKProsthesis, Hip, Cement Restrictor

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2022-11-25
Device Publish Date2022-11-17

Devices Manufactured by TECRES SPA

08031497003894 - InterSpace Hip Trial, 46mm Short2026-02-19
08031497003900 - InterSpace Hip Trial, 54mm Short2026-02-19
08031497003917 - InterSpace Hip Trial, 60mm Short2026-02-19
08031497003924 - InterSpace Hip Trial, 46mm Long 2026-02-19
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

© 2026 FDA.report
This site is not affiliated with or endorsed by the FDA.