FDA UDI In Commercial Distribution 🇺🇸 United States

LUCAS Report Generator

DI: 00883873851913 · Model: 60600 · PHYSIO-CONTROL, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
LUCAS Report Generator
Primary DI
00883873851913
Version / Model
60600
Catalog Number
60600-000145
Company Name
PHYSIO-CONTROL, INC.
Labeler DUNS
009251992
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-08-17
Public Version
3
Public Version Date
2018-11-08
Public Version Status
Update
Public Device Record Key
c960d590-35b3-4256-954a-1fd6ab0bb146

Device Description

SOFTWARE EXECUTABLE, LUCAS Report Generator

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
MR Safe
Direct Marking Exempt
No
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
OUG Medical device data system

GMDN Terms

Code Name
57967 Medical equipment clinical data interfacing software

Identifiers

Type ID
Primary 00883873851913

Customer Contacts