FDA UDI In Commercial Distribution 🇺🇸 United States

K-WIRE,TROCAR POINT 2 END

DI: 00880304359642 · Model: 35-351564 · Biomet Orthopedics, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
K-WIRE,TROCAR POINT 2 END
Primary DI
00880304359642
Version / Model
35-351564
Catalog Number
35-351564
Company Name
Biomet Orthopedics, LLC
Labeler DUNS
129278169
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-26
Public Version
3
Public Version Date
2024-02-19
Public Version Status
Update
Public Device Record Key
424634b5-71f2-433b-b779-cc48e4ef22d5

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
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
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
HTY PIN, FIXATION, SMOOTH

GMDN Terms

Code Name
35685 Orthopaedic bone wire

Identifiers

Type ID
Primary 00880304359642

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify .062 (D) X 9 (L) SNG/ST