FDA UDI In Commercial Distribution 🇺🇸 United States

McKesson

DI: 20612479204366 · Model: 4667 · MCKESSON MEDICAL-SURGICAL INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
50

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Basic Information

Brand Name
McKesson
Primary DI
20612479204366
Version / Model
4667
Company Name
MCKESSON MEDICAL-SURGICAL INC.
Labeler DUNS
023904428
Distribution Status
In Commercial Distribution
Device Count in Pkg
50
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
2a1f45b4-8f34-4efe-a3ca-36e1c383f7a3

Device Description

IV SET, SFTY WINGED 25GX3/4" 1

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
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
FPA Set, Administration, Intravascular

GMDN Terms

Code Name
17825 Scalp vein intravenous administration set

Identifiers

Type ID
Primary 20612479204366
Unit of Use 10612479219752
Package 40612479204377