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FeetMe Monitor FTM-DK

FDA UDI

Class I (US FDA UDI)

by Feetme

Identity

Trade Name
FeetMe Monitor FTM-DK FDA UDI
Generic Name
Pressure monitoring insole FDA UDI
Device Name
FeetMe Monitor Medical device corresponding to a pair of connected insoles Model FTM-DK and version PVT2 FDA UDI
Model / Reference
PVT2 FDA UDI
Description
FeetMe Monitor Medical device corresponding to a pair of connected insoles Model FTM-DK and version PVT2 FDA UDI

Identifiers

Primary DI / UDI-DI
03760349820048 FDA UDI
FDA Product Code
JFC FDA UDI
GMDN Term
Pressure monitoring insole FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.1600 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Pressure monitoring insole

FeetMe Monitor FTM-DK by Feetme — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Pressure monitoring insole.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Feetme

Sources (1)

  • FDA UDI 5d2b2b7f-7b8f-459e-8f19-bf068b1db261 35 fields · synced May 30, 2026