FDA UDI In Commercial Distribution 🇺🇸 United States

Kendall

DI: 10192253040128 · Model: 9250 · Cardinal Health 200, LLC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Kendall
Primary DI
10192253040128
Version / Model
9250
Catalog Number
9250-
Company Name
Cardinal Health 200, LLC
Labeler DUNS
961027315
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-01-19
Public Version
1
Public Version Date
2023-01-27
Public Version Status
New
Public Device Record Key
d7ee5ab3-444a-4408-b9ba-994dd2d80710

Device Description

Kendall Amorphous Hydrogel Wound Dressing

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
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
No
Sterilization Prior Use
No

Product Codes

Code Name
MGQ Dressing, wound and burn, hydrogel w/drug and/or biologic

GMDN Terms

Code Name
47764 Wound hydrogel dressing, non-antimicrobial

Identifiers

Type ID
Package 50192253040126
Primary 10192253040128