FDA UDI In Commercial Distribution 🇺🇸 United States

Kendall

DI: 20884527005403 · Model: 30975232 · Cardinal Health, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Kendall
Primary DI
20884527005403
Version / Model
30975232
Catalog Number
30975232
Company Name
Cardinal Health, Inc.
Labeler DUNS
080935429
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-06-23
Public Version
3
Public Version Date
2019-10-07
Public Version Status
Update
Public Device Record Key
fc5556e9-924a-45ce-88b8-576c40671fb6

Device Description

Tab Belt,Pink and Blue

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
Yes
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
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
FSD BINDER, ABDOMINAL

GMDN Terms

Code Name
10003 Abdominal binder, single-use

Identifiers

Type ID
Package 10884527005406
Primary 20884527005403

Customer Contacts

Device Sizes

Type Value Unit Text
Width 1.5 Inch
Length 40 Inch

Storage Conditions

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