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Endure

FDA UDI

Class I (US FDA UDI)

by Endure Industries, Inc.

Identity

Trade Name
Endure FDA UDI
Generic Name
Oropharyngeal airway, single-use FDA UDI
Device Name
Oropharyngeal Airway, Size 90 mm (Manufacture's Size "3"), Non-Sterile FDA UDI
Model / Reference
OA921217 FDA UDI
Description
Oropharyngeal Airway, Size 90 mm (Manufacture's Size "3"), Non-Sterile FDA UDI

Identifiers

Catalog Number
OA92 FDA UDI
Primary DI / UDI-DI
B531OA920 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

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size
Length — 90 Millimeter FDA UDI

Category: Oropharyngeal airway, single-use

Endure by Endure Industries, Inc. — 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 bbc459e4-e2bc-4ce3-8016-5de9fdfc5d2d 37 fields · synced May 31, 2026