FDA UDI In Commercial Distribution 🇺🇸 United States

VertaPlex

DI: 07613327141818 · Model: 0406422000 · STRYKER CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
VertaPlex
Primary DI
07613327141818
Version / Model
0406422000
Catalog Number
0406422000
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
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
4287188b-4540-4905-9560-daa1b0fac457

Device Description

Half Dose 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

GMDN Terms

Code Name
45253 Orthopaedic cement preparation/delivery kit

Identifiers

Type ID
Package 37613327141819
Primary 07613327141818
Package 57613327141813

Customer Contacts