FDA UDI In Commercial Distribution 🇺🇸 United States

McKesson

DI: 20612479226856 · Model: 178-TB50 · MCKESSON MEDICAL-SURGICAL INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
50

Basic Information

Brand Name
McKesson
Primary DI
20612479226856
Version / Model
178-TB50
Company Name
MCKESSON MEDICAL-SURGICAL INC.
Labeler DUNS
023904428
Distribution Status
In Commercial Distribution
Device Count in Pkg
50
Record Status
Published
Publish Date
2018-02-05
Public Version
4
Public Version Date
2022-06-10
Public Version Status
Update
Public Device Record Key
5f458c8f-1a78-4593-ae3f-e8890b9621a9

Device Description

Immunochemical Fecal Occult Blood Test COLLECTION TUBES

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
Yes
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
KHE Reagent, Occult Blood

GMDN Terms

Code Name
54532 Faecal occult blood IVD, kit, rapid ICT, clinical

Identifiers

Type ID
Primary 20612479226856
Unit of Use 10612479228013