FDA UDI In Commercial Distribution 🇺🇸 United States

Kendall

DI: 10884521175792 · Model: 6651WF · Cardinal Health, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
Kendall
Primary DI
10884521175792
Version / Model
6651WF
Catalog Number
6651WF
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
3
Public Version Date
2021-12-22
Public Version Status
Update
Public Device Record Key
60da4f4c-7189-4c2b-816c-e80fc9c79e20

Device Description

Window Transparent Film Dressing,Moisture Vapor Permeable

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
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
KGX Tape and bandage, adhesive

GMDN Terms

Code Name
58301 Synthetic polymer semi-permeable film dressing, adhesive

Identifiers

Type ID
Package 30884521175796
Primary 10884521175792
Package 20884521175799

Customer Contacts

Device Sizes

Type Value Unit Text
Length 1.75 Inch
Width 1.75 Inch

Storage Conditions

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