FDA UDI In Commercial Distribution 🇺🇸 United States

McKesson

DI: 10612479250182 · Model: 192-PB221W · MCKESSON MEDICAL-SURGICAL INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
McKesson
Primary DI
10612479250182
Version / Model
192-PB221W
Company Name
MCKESSON MEDICAL-SURGICAL INC.
Labeler DUNS
023904428
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-11-18
Public Version
2
Public Version Date
2023-08-17
Public Version Status
Update
Public Device Record Key
4b1cc590-1790-4591-942d-4ff5500ddeb6

Device Description

Catheter, IV safety, push button, sterile, Blue, Winged 22G x 1 in

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
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
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
FOZ Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days

GMDN Terms

Code Name
64574 Peripheral intravenous cannula

Identifiers

Type ID
Package 40612479250206
Package 20612479250196
Primary 10612479250182