FDA UDI In Commercial Distribution 🇺🇸 United States

Kendall

DI: 10192253040111 · Model: 8884476154 · Cardinal Health 200, LLC
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
Kendall
Primary DI
10192253040111
Version / Model
8884476154
Catalog Number
8884476154
Company Name
Cardinal Health 200, LLC
Labeler DUNS
961027315
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-08-14
Public Version
2
Public Version Date
2025-04-17
Public Version Status
Update
Public Device Record Key
9f69cebf-f645-4e43-b4da-8885cab8ad1a

Device Description

Kendall Hydrogel Wound Dressing

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
No
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
NAE Dressing, wound, hydrogel without drug and/or biologic

GMDN Terms

Code Name
47764 Wound hydrogel dressing, non-antimicrobial

Identifiers

Type ID
Package 50192253040119
Package 20192253040118
Primary 10192253040111

Device Sizes

Type Value Unit Text
Width 4.75 Inch