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ArroAir Max Pump Only

FDA UDI

Class II (US FDA UDI)

by Arrowhead Healthcare Supply, Llc

Identity

Trade Name
ArroAir Max Pump Only FDA UDI
Generic Name
Alternating-pressure inflator FDA UDI
Device Name
ArroAir Max Pump Only FDA UDI
Model / Reference
P-108057 FDA UDI
Description
ArroAir Max Pump Only FDA UDI

Identifiers

Primary DI / UDI-DI
00852685007023 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

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

No

FDA UDI

Category: Alternating-pressure inflator

ArroAir Max Pump Only by Arrowhead Healthcare Supply, Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Alternating-pressure inflator.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI ddac4b02-813f-4ec6-b937-e59db669751a 33 fields · synced Jun 8, 2026