FDA UDI In Commercial Distribution 🇺🇸 United States

MULTI-DIRECTIONAL SCREW

DI: 00880304535640 · Model: 131827310 · Biomet Orthopedics, LLC
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
MULTI-DIRECTIONAL SCREW
Primary DI
00880304535640
Version / Model
131827310
Catalog Number
131827310
Company Name
Biomet Orthopedics, LLC
Labeler DUNS
129278169
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-10-24
Public Version
9
Public Version Date
2025-05-30
Public Version Status
Update
Public Device Record Key
01ae0127-7f28-4908-ac1c-ae4428e9a2f8

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
No
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
LXT APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT, METAL COMPOSITE
HRS Plate, fixation, bone

GMDN Terms

Code Name
46646 Orthopaedic bone screw, non-bioabsorbable, sterile

Identifiers

Type ID
Primary 00880304535640

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify 2.7MM X 10MM