FDA UDI In Commercial Distribution 🇺🇸 United States

BIOINTRAFIX

DI: 10886705013418 · Model: 254650 · DEPUY MITEK, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
BIOINTRAFIX
Primary DI
10886705013418
Version / Model
254650
Catalog Number
254650
Company Name
DEPUY MITEK, LLC
Labeler DUNS
190572854
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-01
Public Version
5
Public Version Date
2019-04-23
Public Version Status
Update
Public Device Record Key
81391eba-fd2f-49cd-b65a-78272279762e

Device Description

BIO-INTRAFIX Tibial Sheath Trial For use with BIO-INTRAFIX Implants, T-handle Design 7-8mm

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
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
12696 Orthopaedic implant inserter/extractor, reusable

Identifiers

Type ID
Primary 10886705013418

Customer Contacts