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Ever Ready First Aid

FDA UDI

Class I (US FDA UDI)

by Xiamen Compower Medical Tech. Co., Ltd

Identity

Trade Name
EVER READY FIRST AID FDA UDI
Generic Name
Oropharyngeal airway, single-use FDA UDI
Device Name
Berman airway is used to establish the airway and prevent the tongue fall and the airway block. FDA UDI
Model / Reference
4# FDA UDI
Description
Berman airway is used to establish the airway and prevent the tongue fall and the airway block. FDA UDI

Identifiers

Primary DI / UDI-DI
06946430401052 FDA UDI
FDA Product Code
CAE FDA UDI
GMDN Term
Oropharyngeal airway, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5110 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

Yes

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Oropharyngeal airway, single-use

Ever Ready First Aid by Xiamen Compower Medical Tech. Co., Ltd — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Oropharyngeal airway, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Xiamen Compower Medical Tech. Co., Ltd

Sources (1)

  • FDA UDI 22be9e12-0943-4b30-b753-e7594f183c6f 33 fields · synced May 31, 2026