FDA UDI In Commercial Distribution 🇺🇸 United States

Trial Tibial Augment

DI: 08056269044127 · Model: KZ00505 · ADLER ORTHO SPA
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Trial Tibial Augment
Primary DI
08056269044127
Version / Model
KZ00505
Catalog Number
KZ00505
Company Name
ADLER ORTHO SPA
Labeler DUNS
338847291
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-11-03
Public Version
2
Public Version Date
2026-02-09
Public Version Status
Update
Public Device Record Key
e4ea7ae3-805f-4124-b5ba-22f7adae1c75

Device Description

TRIAL PANTHEON TIBIAL AUGMENT LM/RL SIZE 5 H5

Device Characteristics

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

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
LXH Orthopedic Manual Surgical Instrument

GMDN Terms

Code Name
63524 Knee revision femur/tibia prosthesis trial

Identifiers

Type ID
Primary 08056269044127