FDA UDI In Commercial Distribution 🇺🇸 United States

Revolution

DI: 04546540447838 · Model: 0606514000 · STRYKER CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Revolution
Primary DI
04546540447838
Version / Model
0606514000
Catalog Number
0606514000
Company Name
STRYKER CORPORATION
Labeler DUNS
196548481
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-09-24
Public Version
1
Public Version Date
2018-10-25
Public Version Status
New
Public Device Record Key
06fc86a9-0147-4833-a63f-e5b545a72f9c

Device Description

Femoral Pressurizer Nozzle

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
JDZ MIXER, CEMENT, FOR CLINICAL USE

GMDN Terms

Code Name
47737 Orthopaedic cement injection cannula

Identifiers

Type ID
Package 34546540447839
Primary 04546540447838

Customer Contacts

Device Sizes

Type Value Unit Text
Angle 65.0 degree