FDA UDI In Commercial Distribution 🇺🇸 United States

CARDINAL HEALTH

DI: 10197106540398 · Model: SAN51ADK33 · Cardinal Health 200, LLC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
CARDINAL HEALTH
Primary DI
10197106540398
Version / Model
SAN51ADK33
Catalog Number
SAN51ADK33
Company Name
Cardinal Health 200, LLC
Labeler DUNS
961027315
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-01-16
Public Version
1
Public Version Date
2024-01-24
Public Version Status
New
Public Device Record Key
c0a7328e-ba76-40ed-9ed0-1d6abde317cf

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 50197106540396
Primary 10197106540398

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
15 – 30 Degrees Celsius