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iN∫X®

FDA UDI

Class II (US FDA UDI)

by Ferno-Washington, Inc.

Identity

Trade Name
iN∫X® FDA UDI
Generic Name
Ambulance stretcher, electrohydraulic FDA UDI
Device Name
iN∫X® for iN∫Line™, Integrated Patient Transport & Loading System FDA UDI
Model / Reference
0015803 FDA UDI
Description
iN∫X® for iN∫Line™, Integrated Patient Transport & Loading System FDA UDI

Identifiers

Primary DI / UDI-DI
00190790000004 FDA UDI
FDA Product Code
FPO FDA UDI
GMDN Term
Ambulance stretcher, electrohydraulic FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.6910 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: Ambulance stretcher, electrohydraulic

iN∫X® by Ferno-Washington, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ambulance stretcher, electrohydraulic.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Ferno-Washington, Inc.

Sources (1)

  • FDA UDI 8ede2d3d-2bbb-4093-b0c7-23a35148f1ed 34 fields · synced Jun 9, 2026