FDA UDI In Commercial Distribution 🇺🇸 United States

AXS

DI: 37613327357258 · Model: 56-17334S4 · Stryker Leibinger GmbH & Co. KG
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
4

Basic Information

Brand Name
AXS
Primary DI
37613327357258
Version / Model
56-17334S4
Catalog Number
56-17334S4
Company Name
Stryker Leibinger GmbH & Co. KG
Labeler DUNS
316153956
Distribution Status
In Commercial Distribution
Device Count in Pkg
4
Record Status
Published
Publish Date
2017-05-30
Public Version
4
Public Version Date
2023-09-18
Public Version Status
Update
Public Device Record Key
c5c2812e-ed61-4500-b88e-8578eee9f99d

Device Description

SCREW, AXS, EMERGENCY

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
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
HBW FASTENER, PLATE, CRANIOPLASTY

GMDN Terms

Code Name
46638 Craniofacial bone screw, non-bioabsorbable

Identifiers

Type ID
Primary 37613327357258
Unit of Use 07613327357257

Premarket Submissions

Submission Number Supplement Number
K171152 000

Device Sizes

Type Value Unit Text
Length 4.0 Millimeter
Device Size Text, specify Diameter: 1.7 Millimeter