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Shiley

FDA UDI

Class II (US FDA UDI)

by Covidien LP

Identity

Trade Name
Shiley FDA UDI
Generic Name
Basic endotracheal tube, single-use FDA UDI
Device Name
Nasal RAE Tracheal Tube Cuffless,Murphy Eye FDA UDI
Model / Reference
86287 FDA UDI
Description
Nasal RAE Tracheal Tube Cuffless,Murphy Eye FDA UDI

Identifiers

Primary DI / UDI-DI
30884522006372 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Outer Diameter — 5.0 Millimeter FDA UDI

Category: Basic endotracheal tube, single-use

Shiley by Covidien LP — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Basic endotracheal tube, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Covidien LP

Sources (1)

  • FDA UDI caeabe77-f8df-4038-ac7c-383ca63d6826 35 fields · synced May 31, 2026