FDA UDI In Commercial Distribution 🇺🇸 United States

CARDINAL HEALTH

DI: 10887488721149 · Model: SBA2DEPCFC · Cardinal Health 200, LLC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
CARDINAL HEALTH
Primary DI
10887488721149
Version / Model
SBA2DEPCFC
Catalog Number
SBA2DEPCFC
Company Name
Cardinal Health 200, LLC
Labeler DUNS
961027315
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-05-23
Public Version
3
Public Version Date
2018-07-19
Public Version Status
Update
Public Device Record Key
e6deda47-76d6-4072-b1a9-e71645d7ea1d

Device Description

STRL 624932 EP ABLATION 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 50887488721147
Primary 10887488721149