FDA UDI In Commercial Distribution 🇺🇸 United States

McKesson

DI: 40612479188806 · Model: 569 · MCKESSON MEDICAL-SURGICAL INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
100

Basic Information

Brand Name
McKesson
Primary DI
40612479188806
Version / Model
569
Company Name
MCKESSON MEDICAL-SURGICAL INC.
Labeler DUNS
023904428
Distribution Status
In Commercial Distribution
Device Count in Pkg
100
Record Status
Published
Publish Date
2020-07-21
Public Version
1
Public Version Date
2020-07-29
Public Version Status
New
Public Device Record Key
c1cfaede-d7af-454b-856f-b97bc6d1688e

Device Description

Specimen Container McKesson Polypropylene Screw Cap 120 mL (4 oz.) Sterile

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
Yes
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
No
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
FMH Container, Specimen, Sterile

GMDN Terms

Code Name
58156 Urine transfer IVD, sterile

Identifiers

Type ID
Unit of Use 10612479258904
Primary 40612479188806