FDA UDI In Commercial Distribution 🇺🇸 United States

SpineJack

DI: 03760253800525 · Model: 0909100058 · STRYKER CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
SpineJack
Primary DI
03760253800525
Version / Model
0909100058
Catalog Number
0909-100-058
Company Name
STRYKER CORPORATION
Labeler DUNS
196548481
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-07-27
Public Version
2
Public Version Date
2023-05-03
Public Version Status
Update
Public Device Record Key
7aefd26c-5af4-48fc-8f49-612d532178f7

Device Description

PREPARATION KIT 5.8MM

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
Yes
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
HXG TAMP

GMDN Terms

Code Name
58927 Orthopaedic prosthesis implantation positioning instrument, single-use

Identifiers

Type ID
Primary 03760253800525

Customer Contacts