FDA UDI In Commercial Distribution 🇺🇸 United States

GENTAFIX

DI: 03760177040090 · Model: 1 · TEKNIMED
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
GENTAFIX
Primary DI
03760177040090
Version / Model
1
Catalog Number
T040140G
Company Name
TEKNIMED
Labeler DUNS
764746723
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-09-02
Public Version
3
Public Version Date
2026-01-26
Public Version Status
Update
Public Device Record Key
d96013d9-ad96-4af5-84ee-128ff565cb37

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
No
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
No

Product Codes

Code Name
LOD Bone Cement
MBB Bone Cement, Antibiotic

GMDN Terms

Code Name
46059 Orthopaedic cement, antimicrobial

Identifiers

Type ID
Primary 03760177040090

Storage Conditions

Type
Handling Environment Temperature
Temperature Range
– 25 Degrees Celsius