FDA UDI In Commercial Distribution 🇺🇸 United States

Mckesson

DI: 10612479274973 · Model: MS755 · 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
10612479274973
Version / Model
MS755
Company Name
MCKESSON MEDICAL-SURGICAL INC.
Labeler DUNS
023904428
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-08-28
Public Version
1
Public Version Date
2025-09-05
Public Version Status
New
Public Device Record Key
ba6b153c-9307-419a-9303-4f5dc0adb0a1

Device Description

IV ADMIN SET, 20DRP FLOW REGULATOR 92" (50EA/BX 6BX)

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
58977 Basic intravenous administration set, noninvasive

Identifiers

Type ID
Package 20612479274987
Primary 10612479274973
Package 40612479274998