FDA UDI In Commercial Distribution 🇺🇸 United States

EUROPA™ Pedicle Screw

DI: 00810025483036 · Model: 1-2-10550 · MIRUS LLC
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
EUROPA™ Pedicle Screw
Primary DI
00810025483036
Version / Model
1-2-10550
Company Name
MIRUS LLC
Labeler DUNS
080311078
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-01-27
Public Version
1
Public Version Date
2023-02-06
Public Version Status
New
Public Device Record Key
b5fd1b96-deed-4034-a965-026d34df1cc4

Device Description

Ø10.5 X 50mm EUROPA™ Pedicle Screw

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
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
NKB Thoracolumbosacral Pedicle Screw System
MNH Orthosis, Spondylolisthesis Spinal Fixation
MNI Orthosis, Spinal Pedicle Fixation

GMDN Terms

Code Name
61325 Bone-screw internal spinal fixation system, non-sterile

Identifiers

Type ID
Primary 00810025483036

Premarket Submissions

Submission Number Supplement Number
K180337 000
K182970 000