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Hci Fitness

FDA UDI

Class I (US FDA UDI)

by Healthcare International, Inc.

Identity

Trade Name
Hci Fitness FDA UDI
Generic Name
Mobile patient lifting system, electrically-powered FDA UDI
Device Name
PhysioGait Dynamic Unweighting System PG-600 FDA UDI
Model / Reference
PG-600 FDA UDI
Description
PhysioGait Dynamic Unweighting System PG-600 FDA UDI

Identifiers

Catalog Number
PG-600 FDA UDI
Primary DI / UDI-DI
00850000895157 FDA UDI
FDA Product Code
FSA FDA UDI
GMDN Term
Mobile patient lifting system, electrically-powered FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.5510 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

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Hydrogen Peroxide FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Mobile patient lifting system, electrically-powered

Hci Fitness by Healthcare International, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Healthcare International, Inc.

Sources (1)

  • FDA UDI 1cb01313-8d50-42cd-b743-c9c8dca1159a 34 fields · synced May 30, 2026