FDA UDI In Commercial Distribution 🇺🇸 United States

Kendall

DI: 10192253046359 · Model: 55535 · Cardinal Health 200, LLC
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
Kendall
Primary DI
10192253046359
Version / Model
55535
Catalog Number
55535
Company Name
Cardinal Health 200, LLC
Labeler DUNS
961027315
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-09-08
Public Version
1
Public Version Date
2025-09-16
Public Version Status
New
Public Device Record Key
5d671120-29a3-4930-92f5-ad4a13aa607d

Device Description

Kendall Hydrophillic Foam Dressing Fenestrated 3.5 x 3 in. (8.9 x 7.6 cm)

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
Kit
No
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
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
NAD Dressing, wound, occlusive

GMDN Terms

Code Name
46854 Wound-nonadherent dressing, absorbent, non-antimicrobial

Identifiers

Type ID
Package 50192253046357
Package 20192253046356
Primary 10192253046359

Device Sizes

Type Value Unit Text
Width 7.6 Centimeter
Length 8.9 Centimeter