FDA UDI In Commercial Distribution 🇺🇸 United States

McKesson

DI: 20612479159116 · Model: 73-PP052 · MCKESSON MEDICAL-SURGICAL INC.
Product Codes
2
GMDN Terms
1
Identifiers
3
Pkg Device Count
52

Basic Information

Brand Name
McKesson
Primary DI
20612479159116
Version / Model
73-PP052
Company Name
MCKESSON MEDICAL-SURGICAL INC.
Labeler DUNS
023904428
Distribution Status
In Commercial Distribution
Device Count in Pkg
52
Record Status
Published
Publish Date
2016-12-09
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
a94f2677-dd0a-46e8-8086-d1448820161d

Device Description

TEST SYSTEM, SPORE MAIL-IN (52

Device Characteristics

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

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
MRB Indicator, Biological, Liquid Chemical Sterilization Process
FRC Indicator, Biological Sterilization Process

GMDN Terms

Code Name
13732 Biological sterilization indicator

Identifiers

Type ID
Primary 20612479159116
Unit of Use 10612479159102
Package 40612479159127