FDA UDI In Commercial Distribution 🇺🇸 United States

McKesson

DI: 10612479212562 · Model: 6048 · MCKESSON MEDICAL-SURGICAL INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

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Basic Information

Brand Name
McKesson
Primary DI
10612479212562
Version / Model
6048
Company Name
MCKESSON MEDICAL-SURGICAL INC.
Labeler DUNS
023904428
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-12-09
Public Version
4
Public Version Date
2025-08-18
Public Version Status
Update
Public Device Record Key
c08a506f-89e6-4848-bb1f-773176845a3b

Device Description

IV CATH 22X1

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

GMDN Terms

Code Name
16858 Catheter injection port

Identifiers

Type ID
Primary 10612479212562
Package 20612479212576
Package 40612479212587

Premarket Submissions

Submission Number Supplement Number
K071382 000