← Back to catalogue

Medacure

FDA UDI

Class II (US FDA UDI)

by Medacure Inc

Identity

Trade Name
MEDACURE FDA UDI
Generic Name
Freestanding patient lifting system, electrically-powered FDA UDI
Device Name
FREE SPIRIT FDA UDI
Model / Reference
FS660 FDA UDI
Description
FREE SPIRIT FDA UDI

Identifiers

Primary DI / UDI-DI
00853223008014 FDA UDI
FDA Product Code
FNG FDA UDI
GMDN Term
Freestanding patient lifting system, electrically-powered FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5500 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

Yes

FDA UDI

Category: Freestanding patient lifting system, electrically-powered

Medacure by Medacure Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Freestanding patient lifting system, electrically-powered.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Medacure Inc

Sources (1)

  • FDA UDI 4abdb559-6ae7-4163-b1d0-a97fda34f783 33 fields · synced Jun 6, 2026