FDA UDI In Commercial Distribution 🇺🇸 United States

Kendall

DI: 10192253051841 · Model: 131615 · Cardinal Health 200, LLC
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
Kendall
Primary DI
10192253051841
Version / Model
131615
Catalog Number
131615
Company Name
Cardinal Health 200, LLC
Labeler DUNS
961027315
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-08-13
Public Version
1
Public Version Date
2024-08-21
Public Version Status
New
Public Device Record Key
0c0b71a6-cb78-4963-8f34-6e7905ca7ae4

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 20192253051848
Primary 10192253051841
Package 50192253051849