FDA UDI In Commercial Distribution 🇺🇸 United States

CARDINAL HEALTH

DI: 10195594743970 · Model: SAN36ANTHF · Cardinal Health 200, LLC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
CARDINAL HEALTH
Primary DI
10195594743970
Version / Model
SAN36ANTHF
Catalog Number
SAN36ANTHF
Company Name
Cardinal Health 200, LLC
Labeler DUNS
961027315
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-08-02
Public Version
1
Public Version Date
2022-08-10
Public Version Status
New
Public Device Record Key
abbf594a-2a1d-4561-9059-66e79a03a369

Device Description

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
46408 Cardiothoracic surgical procedure kit, medicated, single-use

Identifiers

Type ID
Package 50195594743978
Primary 10195594743970

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
15 – 30 Degrees Celsius