FDA UDI In Commercial Distribution 🇺🇸 United States

S&W

DI: 10854661006300 · Model: FS-VB011 · Leonhard Lang GmbH
Product Codes
1
GMDN Terms
1
Identifiers
4
Pkg Device Count
25

Basic Information

Brand Name
S&W
Primary DI
10854661006300
Version / Model
FS-VB011
Catalog Number
580
Company Name
Leonhard Lang GmbH
Labeler DUNS
302846407
Distribution Status
In Commercial Distribution
Device Count in Pkg
25
Record Status
Published
Publish Date
2015-10-24
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
80d120f2-83d7-471c-8988-6f8f3b48256a

Device Description

ECG Electrodes

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
Package 30854661006304
Package 20854661006307
Primary 10854661006300
Unit of Use 00854661006303

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
5 – 30 Degrees Celsius