IsoTour

FDA UDI

Class I (US FDA UDI)

by Stryker Corp.

Identity

Trade Name: IsoTour FDA UDI
Generic Name: Alternating-pressure inflator FDA UDI
Model / Reference: 2874 FDA UDI

Identifiers

Catalog Number: 2874-000-001 FDA UDI
Primary DI / UDI-DI: 07613327471427 FDA UDI
FDA Product Code: IKY FDA UDI
FNM FDA UDI
GMDN Term: Alternating-pressure inflator FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 880.5150 FDA UDI
880.5550 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

Yes

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: Alternating-pressure inflator

IsoTour by Stryker Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Alternating-pressure inflator.

DRIVEMEDICAL — Drive Devilbiss Healthcare · Class II
Dolphin Control Unit — Joerns Healthcare · Class II
ArroAir Pro Bariatric 14LPM Pump — ARROWHEAD HEALTHCARE SUPPLY, LLC · Class II
DRIVEMEDICAL — Drive Devilbiss Healthcare · Class II
TurnCair — Joerns Healthcare · Class II
Stratus Pump 5.1 (110 V) — SIZEWISE RENTALS, L.L.C. · Class I
American Bantex — COMPASS HEALTH BRANDS CORP. · Class II
Platinum 6000 Control Unit — SIZEWISE RENTALS, L.L.C. · Class I

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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

Manufacturer

Manufacturer: Stryker Corp.

Sources (1)

FDA UDI d06d797a-4f5c-4f1c-8e13-da3b078b4d22 34 fields · synced Jun 8, 2026