FDA UDI In Commercial Distribution 🇺🇸 United States

SpinePlex

DI: 07613327141788 · Model: 0406202010 · STRYKER CORPORATION
Product Codes
2
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
SpinePlex
Primary DI
07613327141788
Version / Model
0406202010
Catalog Number
0406-202-010
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
5
Public Version Date
2023-03-02
Public Version Status
Update
Public Device Record Key
49737dee-714b-4bac-8692-ad0b1121b39b

Device Description

Radiopaque Bone Cement

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
LON SYSTEM, TEST, AUTOMATED, ANTIMICROBIAL SUSCEPTIBILITY, SHORT INCUBATION

GMDN Terms

Code Name
60505 Vertebral bone filler, non-bioabsorbable

Identifiers

Type ID
Package 37613327141789
Primary 07613327141788
Package 57613327141783

Customer Contacts