FDA UDI In Commercial Distribution 🇺🇸 United States

CARDINAL HEALTH

DI: 10887488566474 · Model: SAN51ADKKA · Cardinal Health 200, LLC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
CARDINAL HEALTH
Primary DI
10887488566474
Version / Model
SAN51ADKKA
Catalog Number
SAN51ADKKA
Company Name
Cardinal Health 200, LLC
Labeler DUNS
961027315
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-08-22
Public Version
3
Public Version Date
2018-07-17
Public Version Status
Update
Public Device Record Key
38acb943-8491-4013-a94e-3f4c3d1a7d7a

Device Description

ANGIO DRAPE PACK MORSE AVE.

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 50887488566472
Primary 10887488566474

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
15 – 30 Degrees Celsius