Freezer Ring

GUDID 08031497001999

Freezer ring is an accessory intended to be applied to the syringe of Mendec Spine Kit. It allows a longer extrusion time of the resin.

TECRES SPA

Orthopaedic cement-chilling device
Primary Device ID08031497001999
NIH Device Record Key3fde3e32-0218-46c9-87e5-a274a875ee55
Commercial Distribution StatusIn Commercial Distribution
Brand NameFreezer Ring
Version Model NumberASB0050
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
GS108031497001999 [Primary]

FDA Product Code

KDDKit, Surgical Instrument, Disposable

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

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.