FDA UDI In Commercial Distribution 🇺🇸 United States

CARDINAL HEALTH

DI: 10197106048450 · Model: SAN12ANK39 · Cardinal Health 200, LLC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
CARDINAL HEALTH
Primary DI
10197106048450
Version / Model
SAN12ANK39
Catalog Number
SAN12ANK39
Company Name
Cardinal Health 200, LLC
Labeler DUNS
961027315
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-12-05
Public Version
1
Public Version Date
2022-12-13
Public Version Status
New
Public Device Record Key
cfe5a8a4-b09b-4827-97e5-5107b35f1eb7

Device Description

CARDIAC DRAPE 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
46408 Cardiothoracic surgical procedure kit, medicated, single-use

Identifiers

Type ID
Package 50197106048458
Primary 10197106048450

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
15 – 30 Degrees Celsius