FDA UDI In Commercial Distribution 🇺🇸 United States

SWAROMED

DI: 19120026223752 · Model: 4023 · TYROLMED GmbH
Product Codes
1
GMDN Terms
1
Identifiers
4
Pkg Device Count
30

Basic Information

Brand Name
SWAROMED
Primary DI
19120026223752
Version / Model
4023
Catalog Number
6001483N
Company Name
TYROLMED GmbH
Labeler DUNS
300387502
Distribution Status
In Commercial Distribution
Device Count in Pkg
30
Record Status
Published
Publish Date
2019-05-03
Public Version
1
Public Version Date
2019-05-13
Public Version Status
New
Public Device Record Key
eaaeb39b-18f7-426d-9641-79987fb01a86

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
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
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 39120026223756
Package 29120026223759
Primary 19120026223752
Unit of Use 09120026223755

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
0 – 40 Degrees Celsius