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AERO HEALTHCARE (US), LLC

US

Last updated May 23, 2026

What AERO HEALTHCARE (US), LLC makes

The company produces single-use cardiopulmonary resuscitation (CPR) masks designed for emergency resuscitation, as well as medicated first aid kits containing pre-packaged medical supplies. Their portfolio also includes a modular device called the Modulator, which appears to be a reusable component for medical applications, and a product named Surefill, likely intended for filling or dispensing medical solutions.

These devices are classified under FDA’s Class I and Class N categories, with listings maintained in the FDA’s Unique Device Identification (UDI) system. The company operates from the United States, adhering to U.S. regulatory requirements for medical devices.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What types of medical devices does Aero Healthcare (US), LLC primarily manufacture?

Aero Healthcare (US), LLC specializes in single-use cardiopulmonary resuscitation (CPR) masks, which are essential for emergency resuscitation. They also produce medicated first aid kits containing pre-packaged medical supplies. Additionally, the company offers a reusable modular device called the Modulator and a product named Surefill, which appears to be designed for filling or dispensing medical solutions. These devices cater to both emergency and general medical care scenarios.

Where is Aero Healthcare (US), LLC based, and how does this affect its regulatory compliance?

Aero Healthcare (US), LLC is based in the United States, meaning its devices must comply with U.S. regulatory requirements, including those set by the FDA. Since the company’s products are listed in the FDA’s Unique Device Identification (UDI) system, they are subject to U.S. medical device regulations, which include classification, labeling, and post-market surveillance standards.

Which regulatory registries or databases list Aero Healthcare’s devices?

Aero Healthcare’s devices are included in the FDA’s Unique Device Identification (UDI) system, which is a centralized database for tracking medical devices in the U.S. This system helps ensure traceability, regulatory compliance, and transparency in the medical device supply chain. The UDI listing is required for devices classified under FDA categories like Class I and Class N.

How are Aero Healthcare’s devices classified under FDA regulations?

Aero Healthcare’s devices fall under FDA’s Class I and Class N classifications. Class I generally includes low-risk devices that pose minimal potential harm to users, such as some single-use CPR masks and first aid kits. Class N specifically refers to non-surgical devices that do not support or sustain human life, do not present a potential unreasonable risk of illness or injury, and are not intended as an accessory to a Class I device. These classifications determine the regulatory oversight and compliance requirements for each product.

What distinguishes Aero Healthcare’s CPR masks and first aid kits from other similar products?

Aero Healthcare’s CPR masks are designed as single-use devices, which reduces the risk of cross-contamination in emergency scenarios. Their medicated first aid kits include pre-packaged medical supplies, likely tailored for quick access in non-emergency situations. The company’s focus on disposable CPR masks and structured first aid kits aligns with FDA’s Class I classification, emphasizing safety and ease of use in critical or routine medical situations. The inclusion of reusable components like the Modulator also suggests versatility in their product portfolio.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
US
Address
—
Website
—
LinkedIn
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Facebook
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Email
—
Phone
—
PRRC Contact
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EUDAMED SRN
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FDA FEI Number
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DUNS Number
008186174

Catalogue (292)

Page 3 of 6
DeviceModel / ReferenceRegistriesClassStatus
Custom AK25AT-238
FDA UDI
NActive
Custom SF25AW-288-01
FDA UDI
NActive
Surefill AK25NR
FDA UDI
NActive
Surefill AKPCPR01
FDA UDI
NActive
Custom AK25ANR-1745
FDA UDI
NActive
Custom AK25W-2050
FDA UDI
NActive
Surefill AKPMBL10
FDA UDI
NActive
Custom SF50BT-2050
FDA UDI
NActive
Custom SS10WM-1732
FDA UDI
NActive
Surefill AK10T
FDA UDI
NActive
Surefill AKP01-2653
FDA UDI
NActive
Custom AK25ANR-1745-01
FDA UDI
NActive
Surefill AK25-SF
FDA UDI
NActive
Surefill SF50AT
FDA UDI
NActive
Custom ADPPK01-351
FDA UDI
NActive
Custom AK25AT-279
FDA UDI
NActive
Custom AKB10W-2050
FDA UDI
NActive
Custom SS25WMCA-71-TY
FDA UDI
NActive
Custom SF25AW-3229
FDA UDI
NActive
Custom AK25AT-1745
FDA UDI
NActive
RapidStop M600-3
FDA UDI
NActive
Custom SS10WM-2169
FDA UDI
NActive
Custom AK10W-2150
FDA UDI
NActive
Modulator M600
FDA UDI
NActive
Custom AK25AW-235-01
FDA UDI
NActive
Surefill AK25AV
FDA UDI
NActive
Custom SF25AW-1840
FDA UDI
NActive
Custom SF50BW-1529
FDA UDI
NActive
Custom AK25NR-233
FDA UDI
NActive
Custom AKBF10W-2832
FDA UDI
NActive
Custom AK10W-2050
FDA UDI
NActive
Surefill AKB50W
FDA UDI
NActive
Custom AK10RSA-1816
FDA UDI
NActive
Custom SF25AW-3115
FDA UDI
NActive
Custom AK10W-2814
FDA UDI
NActive
Custom AK10W-263
FDA UDI
NActive
Surefill AK10-SF
FDA UDI
NActive
Custom AKP01-2050
FDA UDI
NActive
Surefill AKB50-SF
FDA UDI
NActive
Surefill SF25A-SF
FDA UDI
NActive
Custom SF50AW-2790
FDA UDI
NActive
Custom AK75EWN-2437
FDA UDI
NActive
Custom SS10WM-1947-01
FDA UDI
NActive
Custom SF50ANR-2706
FDA UDI
NActive
Custom AK10W-317
FDA UDI
NActive
Surefill SF50BT
FDA UDI
NActive
Custom AK25AW-002
FDA UDI
NActive
Custom SSBK25-71
FDA UDI
NActive
Custom AK25AT-287
FDA UDI
NActive
Surefill AKPEI01
FDA UDI
NActive

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