FDA UDI In Commercial Distribution 🇺🇸 United States

SKINTACT

DI: 19005531001128 · Model: RT38 · Leonhard Lang GmbH
Product Codes
1
GMDN Terms
1
Identifiers
4
Pkg Device Count
100

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Basic Information

Brand Name
SKINTACT
Primary DI
19005531001128
Version / Model
RT38
Catalog Number
RT38
Company Name
Leonhard Lang GmbH
Labeler DUNS
302846407
Distribution Status
In Commercial Distribution
Device Count in Pkg
100
Record Status
Published
Publish Date
2024-07-24
Public Version
1
Public Version Date
2024-08-01
Public Version Status
New
Public Device Record Key
0f32fee7-e8c8-4ebf-a17e-ad7d82e9cf9b

Device Description

ECG 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
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 29005531001125
Primary 19005531001128
Package 39005531001122
Unit of Use 09005531001121

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
5 – 30 Degrees Celsius