FDA UDI In Commercial Distribution 🇺🇸 United States

K-WIRE TROCAR POINT

DI: 00880304648678 · Model: IFI-491414 · Biomet Orthopedics, LLC
Product Codes
2
GMDN Terms
1
Identifiers
2
Pkg Device Count
6

Basic Information

Brand Name
K-WIRE TROCAR POINT
Primary DI
00880304648678
Version / Model
IFI-491414
Catalog Number
IFI-491414
Company Name
Biomet Orthopedics, LLC
Labeler DUNS
129278169
Distribution Status
In Commercial Distribution
Device Count in Pkg
6
Record Status
Published
Publish Date
2020-03-30
Public Version
2
Public Version Date
2024-02-19
Public Version Status
Update
Public Device Record Key
b1383667-1bdb-4780-b7b0-84e5b42a88c0

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
HRS Plate, fixation, bone
HWC Screw, fixation, bone

GMDN Terms

Code Name
35685 Orthopaedic bone wire

Identifiers

Type ID
Unit of Use 30880304648679
Primary 00880304648678

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K110201 000

Device Sizes

Type Value Unit Text
Device Size Text, specify .045 INCH X 4.72 INCH