FDA UDI In Commercial Distribution 🇺🇸 United States

TRIO TRAUMA

DI: 04546540683137 · Model: 47110425 · Stryker Corporation
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
TRIO TRAUMA
Primary DI
04546540683137
Version / Model
47110425
Catalog Number
47110425
Company Name
Stryker Corporation
Labeler DUNS
149183167
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2014-12-08
Public Version
6
Public Version Date
2023-06-21
Public Version Status
Update
Public Device Record Key
e0c61c0f-73d5-46d4-b95e-f595c566add3

Device Description

CANNULATED 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
Yes
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 Orthosis, spinal pedicle fixation, for degenerative disc disease
MNI ORTHOSIS, SPINAL PEDICLE FIXATION
MNH Orthosis, spondylolisthesis spinal fixation

GMDN Terms

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

Identifiers

Type ID
Primary 04546540683137

Device Sizes

Type Value Unit Text
Length 25.0 Millimeter
Device Size Text, specify Diameter: 4.5 Millimeter