FDA UDI In Commercial Distribution 🇺🇸 United States

XIA PRECISION

DI: 07613327265026 · Model: 48230230 · Stryker Corporation
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
XIA PRECISION
Primary DI
07613327265026
Version / Model
48230230
Catalog Number
48230230
Company Name
Stryker Corporation
Labeler DUNS
149183167
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-12-16
Public Version
3
Public Version Date
2023-09-18
Public Version Status
Update
Public Device Record Key
9a2de20f-d4cc-496e-a7d8-8d5b8d7af967

Device Description

K-WIRE SHARP

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
Yes
PM Exempt
Yes
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
LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

GMDN Terms

Code Name
63819 Spinal guidewire

Identifiers

Type ID
Primary 07613327265026

Device Sizes

Type Value Unit Text
Device Size Text, specify Diameter: 1.3 Millimeter