FDA UDI In Commercial Distribution 🇺🇸 United States

PCD

DI: 04546540907073 · Model: 0506489000 · STRYKER CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
PCD
Primary DI
04546540907073
Version / Model
0506489000
Catalog Number
0506489000
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
f380ba0f-5de7-4aa2-a11c-62b19aa48cbe

Device Description

Precision System Kit with Short Extension Tube

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
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)

GMDN Terms

Code Name
33191 Manual orthopaedic cement mixer, reusable

Identifiers

Type ID
Package 34546540907074
Primary 04546540907073

Customer Contacts