FDA UDI In Commercial Distribution 🇺🇸 United States

CARDINAL HEALTH

DI: 10197106539309 · Model: SAN3JAPK17 · Cardinal Health 200, LLC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
CARDINAL HEALTH
Primary DI
10197106539309
Version / Model
SAN3JAPK17
Catalog Number
SAN3JAPK17
Company Name
Cardinal Health 200, LLC
Labeler DUNS
961027315
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-01-03
Public Version
1
Public Version Date
2024-01-11
Public Version Status
New
Public Device Record Key
bd94851e-72d5-45e8-9b0e-880a52d86226

Device Description

ANGIOGRAPHY PACK 2

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 50197106539307
Primary 10197106539309

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
15 – 30 Degrees Celsius