FDA UDI In Commercial Distribution 🇺🇸 United States

CARDINAL HEALTH

DI: 10197106990056 · Model: SAN69CPWH2 · 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
10197106990056
Version / Model
SAN69CPWH2
Catalog Number
SAN69CPWH2
Company Name
Cardinal Health 200, LLC
Labeler DUNS
961027315
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-03-20
Public Version
1
Public Version Date
2025-03-28
Public Version Status
New
Public Device Record Key
7203033f-9b2f-47be-b0a5-5282992c1dbc

Device Description

CATH LAB PROCEDURE 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
61371 Cardiothoracic surgical procedure kit, non-medicated, single-use

Identifiers

Type ID
Package 50197106990054
Primary 10197106990056

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
15 – 30 Degrees Celsius