FDA UDI In Commercial Distribution 🇺🇸 United States

Kendall

DI: 10884521065802 · Model: 55535AMDX · Cardinal Health, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Kendall
Primary DI
10884521065802
Version / Model
55535AMDX
Catalog Number
55535AMDX-
Company Name
Cardinal Health, Inc.
Labeler DUNS
080935429
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-06-13
Public Version
1
Public Version Date
2023-06-21
Public Version Status
New
Public Device Record Key
f7efce3c-a282-407c-95dd-9735b47a03c2

Device Description

Kendall AMD Antimicrobial Fenestrated Foam Dressing

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
Yes
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
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
FRO Dressing, wound, drug

GMDN Terms

Code Name
47042 Wound-nonadherent dressing, absorbent, antimicrobial

Identifiers

Type ID
Package 20884521065809
Primary 10884521065802