FDA UDI In Commercial Distribution 🇺🇸 United States

Kendall

DI: 10192253051858 · Model: 139090 · Cardinal Health 200, LLC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

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Basic Information

Brand Name
Kendall
Primary DI
10192253051858
Version / Model
139090
Catalog Number
139090
Company Name
Cardinal Health 200, LLC
Labeler DUNS
961027315
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-08-14
Public Version
1
Public Version Date
2024-08-22
Public Version Status
New
Public Device Record Key
5aa09fa9-393b-4787-988b-881c137a9250

Device Description

Scalpel

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
No
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
GDX SCALPEL, ONE-PIECE

GMDN Terms

Code Name
37445 Manual scalpel blade, single-use

Identifiers

Type ID
Package 50192253051856
Primary 10192253051858