FDA UDI In Commercial Distribution 🇺🇸 United States

McKesson

DI: 10612479272269 · Model: 419-64125 · MCKESSON MEDICAL-SURGICAL INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

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Basic Information

Brand Name
McKesson
Primary DI
10612479272269
Version / Model
419-64125
Company Name
MCKESSON MEDICAL-SURGICAL INC.
Labeler DUNS
023904428
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-08-21
Public Version
1
Public Version Date
2024-08-29
Public Version Status
New
Public Device Record Key
b4b2702f-9f35-44d1-97d4-753df3203284

Device Description

BAG, EVA GRAVITY 3LEG 2000ML (50/CS)

Device Characteristics

Single Use
No
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
KPE Container, I.V.

GMDN Terms

Code Name
15808 Evacuated intravenous fluid container

Identifiers

Type ID
Package 40612479272277
Primary 10612479272269

Premarket Submissions

Submission Number Supplement Number
K030888 000