FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 10653405001126 · Model: 01-4130 · Conmed Corporation
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
50

Basic Information

Brand Name
NA
Primary DI
10653405001126
Version / Model
01-4130
Catalog Number
01-4130
Company Name
Conmed Corporation
Labeler DUNS
071595540
Distribution Status
In Commercial Distribution
Device Count in Pkg
50
Record Status
Published
Publish Date
2016-09-24
Public Version
4
Public Version Date
2024-02-19
Public Version Status
Update
Public Device Record Key
b60f27d3-8a34-40e0-ae71-20b6aca7ea81

Device Description

INFANT ECG BACKPAD

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
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
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
Package 20653405001123
Primary 10653405001126
Unit of Use 00653405001129

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K960264 000

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
41 – 95 Degrees Fahrenheit
Type
Storage Environment Temperature
Temperature Range
5 – 35 Degrees Celsius
Type
Storage Environment Humidity
Temperature Range
30 – 75 Percent (%) Relative Humidity