FDA UDI In Commercial Distribution 🇺🇸 United States

ASNIS

DI: 07613153051749 · Model: 606135 · Stryker Trauma SA
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ASNIS
Primary DI
07613153051749
Version / Model
606135
Catalog Number
606135
Company Name
Stryker Trauma SA
Labeler DUNS
481999654
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-24
Public Version
6
Public Version Date
2024-02-19
Public Version Status
Update
Public Device Record Key
811e49fe-a234-4a73-82bb-8d83f30bac6a

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
MR Conditional
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
HWC Screw, fixation, bone

GMDN Terms

Code Name
66947 Orthopaedic bone screw (non-sliding)

Identifiers

Type ID
Primary 07613153051749

Premarket Submissions

Submission Number Supplement Number
K024060 000

Device Sizes

Type Value Unit Text
Device Size Text, specify Diameter: 6.5 Millimeter
Length 135.0 Millimeter