FDA UDI In Commercial Distribution 🇺🇸 United States

Kendall

DI: 30884521024827 · Model: 9232 · Cardinal Health, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
Kendall
Primary DI
30884521024827
Version / Model
9232
Catalog Number
9232
Company Name
Cardinal Health, Inc.
Labeler DUNS
080935429
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-06-30
Public Version
5
Public Version Date
2021-07-22
Public Version Status
Update
Public Device Record Key
65c029a2-1e98-47dc-9931-c1eec44b4e92

Device Description

Calcium Alginate 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
No
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
KMF Bandage, liquid

GMDN Terms

Code Name
43186 Exudate-absorbent dressing, hydrophilic-gel, non-antimicrobial

Identifiers

Type ID
Package 20884521024820
Primary 30884521024827
Package 10884521024823

Customer Contacts

Device Sizes

Type Value Unit Text
Length 2 Inch
Width 2 Inch

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Keep dry;AVOID DIRECT SUNLIGHT