FDA UDI In Commercial Distribution 🇺🇸 United States

CARDINAL HEALTH

DI: 10197106806579 · Model: SAN21AO62H · Cardinal Health 200, LLC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
CARDINAL HEALTH
Primary DI
10197106806579
Version / Model
SAN21AO62H
Catalog Number
SAN21AO62H
Company Name
Cardinal Health 200, LLC
Labeler DUNS
961027315
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-11-18
Public Version
1
Public Version Date
2024-11-26
Public Version Status
New
Public Device Record Key
da990b3c-17bd-4db0-a7fe-c50c58943f00

Device Description

AOG ANGIO PACK

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 50197106806577
Primary 10197106806579

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
15 – 30 Degrees Celsius