FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 04546540857880 · Model: 0206530000 · STRYKER CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
04546540857880
Version / Model
0206530000
Catalog Number
0206530000
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
9b28c87c-11dd-4cff-9b4d-3bf1dd1c9580

Device Description

Cartridge with Breakaway Femoral 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 34546540857881
Primary 04546540857880

Customer Contacts

Device Sizes

Type Value Unit Text
Weight 180.0 Gram