FDA UDI Not in Commercial Distribution 🇺🇸 United States

LEADER

DI: 00096295130362 · Model: 5297460 · Cardinal Health 110, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
4
Pkg Device Count
3

Basic Information

Brand Name
LEADER
Primary DI
00096295130362
Version / Model
5297460
Catalog Number
5297460
Company Name
Cardinal Health 110, Inc.
Labeler DUNS
063997360
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
3
Record Status
Published
Publish Date
2017-04-14
Public Version
5
Public Version Date
2022-10-12
Public Version Status
Update
Public Device Record Key
00c9e568-7937-49f1-b548-2f49d4e8ab6b
Distribution End Date
2022-10-11

Device Description

LDR Electro TENS replacement gel pads 3 ea

Device Characteristics

Single Use
No
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
No
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
NUH STIMULATOR, NERVE, TRANSCUTANEOUS, OVER-THE-COUNTER

GMDN Terms

Code Name
35372 Analgesic transcutaneous electrical nerve stimulation system

Identifiers

Type ID
Package 30096295130363
Primary 00096295130362
Package 50096295130367
Unit of Use 10096295130369

Customer Contacts

Storage Conditions

Type
Storage Environment Humidity
Temperature Range
30 – 95 Percent (%) Relative Humidity
Type
Storage Environment Temperature
Temperature Range
-10 – 60 Degrees Celsius