FDA UDI Not in Commercial Distribution 🇺🇸 United States

NA

DI: 10653405006220 · Model: LMC 101 · Conmed Corporation
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
600

Basic Information

Brand Name
NA
Primary DI
10653405006220
Version / Model
LMC 101
Catalog Number
LMC 101
Company Name
Conmed Corporation
Labeler DUNS
071595540
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
600
Record Status
Published
Publish Date
2017-04-03
Public Version
4
Public Version Date
2021-03-26
Public Version Status
Update
Public Device Record Key
9366074c-0760-41b5-b2e7-b82e75efafcd
Distribution End Date
2021-03-25

Device Description

RADIOLUCENT ELECTRODE

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 30653405006224
Primary 10653405006220
Unit of Use 00653405006223

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K890201 000