FDA UDI In Commercial Distribution 🇺🇸 United States

CARDINAL HEALTH

DI: 10198956319202 · Model: SAN23AD112 · Cardinal Health 200, LLC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
CARDINAL HEALTH
Primary DI
10198956319202
Version / Model
SAN23AD112
Catalog Number
SAN23AD112
Company Name
Cardinal Health 200, LLC
Labeler DUNS
961027315
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2026-01-30
Public Version
1
Public Version Date
2026-02-09
Public Version Status
New
Public Device Record Key
bea61fb8-0a3c-49c7-af8f-a3ac08c65860

Device Description

ANGIO DRAPE PACK NEURO

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
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
Yes
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
OEQ Angiography/angioplasty kit

GMDN Terms

Code Name
16545 Angiography kit

Identifiers

Type ID
Package 50198956319200
Primary 10198956319202

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
High: 40 Degrees Celsius