FDA UDI In Commercial Distribution 🇺🇸 United States

Medline

DI: 20197344049889 · Model: MDSLFSVM01 · MEDLINE INDUSTRIES, INC.
Product Codes
1
GMDN Terms
1
Identifiers
4
Pkg Device Count
30

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Basic Information

Brand Name
Medline
Primary DI
20197344049889
Version / Model
MDSLFSVM01
Catalog Number
MDSLFSVM01
Company Name
MEDLINE INDUSTRIES, INC.
Labeler DUNS
025460908
Distribution Status
In Commercial Distribution
Device Count in Pkg
30
Record Status
Published
Publish Date
2024-03-27
Public Version
1
Public Version Date
2024-04-04
Public Version Status
New
Public Device Record Key
66d55325-1214-48ba-96af-e8d52b7d6384

Device Description

ELECTRODE,FOAM,WETGEL,OFFSET,SNAP,TAB

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
Yes
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 30197344049886
Package 40197344049883
Primary 20197344049889
Unit of Use 10197344049882

Customer Contacts

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
5 – 30 Degrees Celsius
Type
Special Storage Condition, Specify
Special Conditions
Protect from freezing, avoid excessive heat.Keep away from sunlight.Keep Dry.