FDA UDI Not in Commercial Distribution 🇺🇸 United States

PCD

DI: 04546540906991 · Model: 0506482000 · STRYKER CORPORATION
Product Codes
2
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
PCD
Primary DI
04546540906991
Version / Model
0506482000
Catalog Number
0506-482-000
Company Name
STRYKER CORPORATION
Labeler DUNS
196548481
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-09-24
Public Version
2
Public Version Date
2021-10-25
Public Version Status
Update
Public Device Record Key
04eebd22-ad0d-45cd-ac70-6bd8042ca89e
Distribution End Date
2021-07-09

Device Description

Precision System with Needle

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
OAR Injector, vertebroplasty (does not contain cement)
JDZ MIXER, CEMENT, FOR CLINICAL USE

GMDN Terms

Code Name
45253 Orthopaedic cement preparation/delivery kit

Identifiers

Type ID
Package 34546540906992
Primary 04546540906991

Customer Contacts

Device Sizes

Type Value Unit Text
Needle Gauge 10.0 Gauge