FDA UDI Not in Commercial Distribution 🇺🇸 United States

Kendall

DI: 10884521021921 · Model: 9256 · Cardinal Health, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
Kendall
Primary DI
10884521021921
Version / Model
9256
Catalog Number
9256
Company Name
Cardinal Health, Inc.
Labeler DUNS
080935429
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-06-27
Public Version
6
Public Version Date
2023-04-17
Public Version Status
Update
Public Device Record Key
229ebd60-b9b6-4792-9fea-1e4f2d3cfb9b
Distribution End Date
2023-04-15

Device Description

Hydrogel Impregnated Gauze,USP Type VII Gauze Pad 1.0 oz (30 mL) Gel

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
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 20884521021928
Primary 10884521021921
Package 30884521021925

Device Sizes

Type Value Unit Text
Length 4 Inch
Total Volume 30 Milliliter
Width 4 Inch

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
This side up;