FDA UDI In Commercial Distribution 🇺🇸 United States

CARDINAL HEALTH

DI: 10887488982434 · Model: SAN23BS675 · Cardinal Health 200, LLC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
CARDINAL HEALTH
Primary DI
10887488982434
Version / Model
SAN23BS675
Catalog Number
SAN23BS675
Company Name
Cardinal Health 200, LLC
Labeler DUNS
961027315
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-05-02
Public Version
2
Public Version Date
2018-07-23
Public Version Status
Update
Public Device Record Key
baea6afe-e9d4-4e68-bb7e-c48a48ffc67f

Device Description

ANGIO/INTERVENT TRAY

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 50887488982432
Primary 10887488982434

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
15 – 30 Degrees Celsius