FDA UDI In Commercial Distribution 🇺🇸 United States

SpinePlex

DI: 07613327141771 · Model: 0406222000 · STRYKER CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
SpinePlex
Primary DI
07613327141771
Version / Model
0406222000
Catalog Number
0406222000
Company Name
STRYKER CORPORATION
Labeler DUNS
196548481
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-23
Public Version
3
Public Version Date
2020-06-19
Public Version Status
Update
Public Device Record Key
e7a6f00c-45e0-4874-9b4d-ba886f60a9b4

Device Description

Half Dose

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
NDN CEMENT, BONE, VERTEBROPLASTY

GMDN Terms

Code Name
35217 Orthopaedic cement, non-antimicrobial

Identifiers

Type ID
Package 57613327141776
Package 37613327141772
Primary 07613327141771

Customer Contacts