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Allied Medical LLC

FDA UDI

Class II (US FDA UDI)

by Allied Medical LLC

Identity

Trade Name
Allied Medical LLC FDA UDI
Generic Name
Transport electric ventilator FDA UDI
Device Name
Ventilator Mass Casualty FDA UDI
Model / Reference
AHP300P FDA UDI
Description
Ventilator Mass Casualty FDA UDI

Identifiers

Catalog Number
AHP300P FDA UDI
Primary DI / UDI-DI
00026072000083 FDA UDI
510(k) Number
K131098 FDA UDI
FDA Product Code
BTL FDA UDI
GMDN Term
Transport electric ventilator FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5925 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

Yes

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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Transport electric ventilator

Allied Medical LLC by Allied Medical LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Transport electric ventilator.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Allied Medical LLC

Sources (1)

  • FDA UDI 677172a9-1df5-464b-b438-cf39fe6d0056 35 fields · synced Jun 6, 2026