FDA UDI Not in Commercial Distribution 🇺🇸 United States

S2

DI: 07613153292012 · Model: 1732-1334S · Stryker Trauma GmbH
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
S2
Primary DI
07613153292012
Version / Model
1732-1334S
Catalog Number
1732-1334S
Company Name
Stryker Trauma GmbH
Labeler DUNS
330211587
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-24
Public Version
7
Public Version Date
2025-02-06
Public Version Status
Update
Public Device Record Key
bf041c99-dbc0-4196-98dd-f4ebef6147eb
Distribution End Date
2021-07-27

Device Description

Femoral Nail, A,R

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
HSB ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES

GMDN Terms

Code Name
33187 Femur intramedullary nail

Identifiers

Type ID
Primary 07613153292012

Device Sizes

Type Value Unit Text
Device Size Text, specify Diameter: 13.0 Millimeter
Length 340.0 Millimeter