FDA UDI In Commercial Distribution 🇺🇸 United States

McKesson

DI: 10612479183114 · Model: 87-320 · MCKESSON MEDICAL-SURGICAL INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
50

Basic Information

Brand Name
McKesson
Primary DI
10612479183114
Version / Model
87-320
Company Name
MCKESSON MEDICAL-SURGICAL INC.
Labeler DUNS
023904428
Distribution Status
In Commercial Distribution
Device Count in Pkg
50
Record Status
Published
Publish Date
2016-12-09
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
17b62d99-4d23-4fc5-9bcc-0c8ca6a037c5

Device Description

ELECTRODE, EKG ALL-PURP TAPE S

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
Yes
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
DRX Electrode, Electrocardiograph

GMDN Terms

Code Name
35035 Electrocardiographic electrode, single-use

Identifiers

Type ID
Primary 10612479183114
Unit of Use 00612479219038
Package 40612479183122