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Equipoise

FDA UDI

Class I (US FDA UDI)

by Equidor Medtech Llp

Identity

Trade Name
EQUIPOISE FDA UDI
Generic Name
Posturography system FDA UDI
Device Name
Device with hardware comprising a force plate and software for analysis of center of pressure during static and dynamic tests of stance. FDA UDI
Model / Reference
EQPOS FDA UDI
Description
Device with hardware comprising a force plate and software for analysis of center of pressure during static and dynamic tests of stance. FDA UDI

Identifiers

Primary DI / UDI-DI
08908024776005 FDA UDI
FDA Product Code
KHX FDA UDI
GMDN Term
Posturography system FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.1575 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

Yes

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Posturography system

Equipoise by Equidor Medtech Llp — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Posturography system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Equidor Medtech Llp

Sources (1)

  • FDA UDI ddde370b-3dc4-4a6f-8474-c36051064e1a 34 fields · synced May 30, 2026