FDA UDI In Commercial Distribution 🇺🇸 United States

Footswitch

DI: EMTDE104201USMP0 · Model: E104201USMP · MT.DERM GmbH
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Footswitch
Primary DI
EMTDE104201USMP0
Version / Model
E104201USMP
Company Name
MT.DERM GmbH
Labeler DUNS
329216357
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-01-01
Public Version
5
Public Version Date
2023-11-03
Public Version Status
Update
Public Device Record Key
283c57ab-2735-4bc0-ab73-690fa0ee6f4e

Device Description

The Footswitch is an accessory of Exceed.

Device Characteristics

Single Use
No
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
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
QAI Powered Microneedle Device

GMDN Terms

Code Name
61216 Cosmetic micro-needling electronic handpiece, professional

Identifiers

Type ID
Primary EMTDE104201USMP0
Package EMTDE104201USMP1

Storage Conditions

Type
Handling Environment Temperature
Temperature Range
59 – 77 Degrees Fahrenheit
Type
Storage Environment Humidity
Temperature Range
10 – 90 Percent (%) Relative Humidity
Type
Handling Environment Humidity
Temperature Range
30 – 75 Percent (%) Relative Humidity
Type
Storage Environment Temperature
Temperature Range
14 – 104 Degrees Fahrenheit
Type
Storage Environment Atmospheric Pressure
Temperature Range
54 – 107 KiloPascal
Type
Handling Environment Atmospheric Pressure
Temperature Range
60 – 107 KiloPascal