FDA UDI In Commercial Distribution 🇺🇸 United States

PROFYLE

DI: 37613153150108 · Model: 59-23026 · Stryker Trauma SA
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
5

Basic Information

Brand Name
PROFYLE
Primary DI
37613153150108
Version / Model
59-23026
Catalog Number
59-23026
Company Name
Stryker Trauma SA
Labeler DUNS
481999654
Distribution Status
In Commercial Distribution
Device Count in Pkg
5
Record Status
Published
Publish Date
2015-09-24
Public Version
7
Public Version Date
2024-02-19
Public Version Status
Update
Public Device Record Key
840fd185-c1cd-48a5-b0b0-3bc2a0a1b4ca

Device Description

BONE SCREWS, CROSS-FIT, SELF-TAPPING

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
HRS PLATE, FIXATION, BONE

GMDN Terms

Code Name
66947 Orthopaedic bone screw (non-sliding)

Identifiers

Type ID
Primary 37613153150108
Unit of Use 07613153150107

Device Sizes

Type Value Unit Text
Device Size Text, specify Diameter: 2.3 Millimeter
Length 26.0 Millimeter