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Ever Ready

FDA UDI

Class I (US FDA UDI)

by Xiamen Compower Medical Tech. Co., Ltd

Identity

Trade Name
Ever Ready 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
S40/S60/S80/S90/S100/S110 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
06946430403773 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 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

Sources (1)

  • FDA UDI 8a680bf9-9dce-4be6-8261-29b000fbf629 33 fields · synced May 30, 2026