FDA UDI Not in Commercial Distribution 🇺🇸 United States

CORE

DI: 04546540427359 · Model: 5400500000 · STRYKER CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
CORE
Primary DI
04546540427359
Version / Model
5400500000
Catalog Number
5400-500-000
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
3
Public Version Date
2019-12-30
Public Version Status
Update
Public Device Record Key
178f8c14-e59f-4b09-91e6-198d8e99e92c
Distribution End Date
2018-12-31

Device Description

Heavy Duty Power Pack

Device Characteristics

Single Use
No
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
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
HWE INSTRUMENT, SURGICAL, ORTHOPEDIC, AC-POWERED MOTOR AND ACCESSORY/ATTACHMENT

GMDN Terms

Code Name
35102 Surgical helmet system

Identifiers

Type ID
Primary 04546540427359

Customer Contacts

Storage Conditions

Type
Storage Environment Atmospheric Pressure
Temperature Range
50 – 106 KiloPascal
Type
Storage Environment Temperature
Temperature Range
-20 – 40 Degrees Celsius
Type
Storage Environment Humidity
Temperature Range
10 – 75 Percent (%) Relative Humidity