Arise 1000 EX

FDA UDI

Class II (US FDA UDI)

by Joerns Healthcare

Identity

Trade Name: Arise 1000 EX FDA UDI
Generic Name: Alternating-pressure inflator FDA UDI
Model / Reference: AREXLAL-CU FDA UDI

Identifiers

Catalog Number: AREXLAL-CU FDA UDI
Primary DI / UDI-DI: 00857268006608 FDA UDI
FDA Product Code: FNM FDA UDI
GMDN Term: Alternating-pressure inflator FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 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

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

Arise 1000 EX by Joerns Healthcare — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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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 II	Pending data

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Manufacturer

Manufacturer: Joerns Healthcare

Sources (1)

FDA UDI 100a761d-da9a-451c-9b18-f714d41aef6d 33 fields · synced Jun 9, 2026