FDA UDI In Commercial Distribution 🇺🇸 United States

Genex Bone Graft Substitute

DI: 15060155711475 · Model: 910-003Z · BIOCOMPOSITES LTD
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Genex Bone Graft Substitute
Primary DI
15060155711475
Version / Model
910-003Z
Catalog Number
910-003Z
Company Name
BIOCOMPOSITES LTD
Labeler DUNS
424382307
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-02-17
Public Version
1
Public Version Date
2022-02-25
Public Version Status
New
Public Device Record Key
1200e022-7b57-4c10-8fb9-fdd9b74654c6

Device Description

genex® Bone Graft Substitute is a simple to use synthetic absorbable material designed to promote regeneration of bone in osseous defects. It degrades into component elements normally found in the body and is highly biocompatible. The kit contains a powder filled syringe and mixing solution which, when combined, provides a mouldable cohesive paste which may be implanted into open voids/gaps of the musculoskeletal system to set in situ or placed in the bead mould mat provided to form beads for implantation. When injected the mixture sets to form genex® Bone Graft substitute a hard but absorbable matrix. genex® Bone Graft Substitute is supplied sterile. genex® Bone Graft Substitute , accessories and packaging are not made from natural rubber latex. genex® Bone Graft Substitute is MR safe.

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
Yes
MRI Safety
MR Safe
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
Yes
Sterilization Methods
Radiation Sterilization

Product Codes

Code Name
MQV Filler, Bone Void, Calcium Compound

GMDN Terms

Code Name
16966 Synthetic bone graft

Identifiers

Type ID
Primary 15060155711475

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K212721 000