← Back to catalogue

RediTube™

FDA UDI

Class II (US FDA UDI)

by Airlife, Inc.

Identity

Trade Name
RediTube™ FDA UDI
Generic Name
Basic endotracheal tube, single-use FDA UDI
Device Name
Tracheal Tube Oral/Nasal with Pre-loaded Stylet FDA UDI
Model / Reference
8040RTC FDA UDI
Description
Tracheal Tube Oral/Nasal with Pre-loaded Stylet FDA UDI

Identifiers

Catalog Number
8040RTC FDA UDI
Primary DI / UDI-DI
10190752152366 FDA UDI
510(k) Number
K042683 FDA UDI
FDA Product Code
BTR FDA UDI
GMDN Term
Basic endotracheal tube, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5730 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Basic endotracheal tube, single-use

RediTube™ by Airlife, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Basic endotracheal tube, single-use.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Airlife, Inc.

Sources (1)

  • FDA UDI 80d967ab-f437-434e-be5f-c9d614d117b3 37 fields · synced May 31, 2026