FDA UDI In Commercial Distribution 🇺🇸 United States

Truliant CC

DI: 10885862627445 · Model: 02-019-30-0202 · Exactech, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Truliant CC
Primary DI
10885862627445
Version / Model
02-019-30-0202
Catalog Number
02-019-30-0202
Company Name
Exactech, Inc.
Labeler DUNS
157565946
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-11-09
Public Version
1
Public Version Date
2023-11-17
Public Version Status
New
Public Device Record Key
7b46fcc0-579a-40d4-8b4b-56729f3bc867

Device Description

TRULIANT TIBIAL OFFSET PREP REAMER

Device Characteristics

Single Use
No
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
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
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
JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER

GMDN Terms

Code Name
45114 Bone-resection orthopaedic reamer, reusable

Identifiers

Type ID
Primary 10885862627445

Premarket Submissions

Submission Number Supplement Number
K150890 000