FDA UDI In Commercial Distribution 🇺🇸 United States

Kendall

DI: 20884527005359 · Model: 30950292 · Cardinal Health, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Kendall
Primary DI
20884527005359
Version / Model
30950292
Catalog Number
30950292
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
86811810-38a3-428f-989e-81ae13b5059f

Device Description

Buttonhole Belt,Pink and Blue Striped

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 10884527005352
Primary 20884527005359

Customer Contacts

Device Sizes

Type Value Unit Text
Width 2.375 Inch
Length 48 Inch

Storage Conditions

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