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Hudson Rci

FDA UDI

Class II (US FDA UDI)

by Teleflex Incorporated

Identity

Trade Name
HUDSON RCI FDA UDI
Generic Name
Endotracheal tube guide, single-use FDA UDI
Device Name
ET TUBE, EXCHANGER, ETX, 35 - 41 FR FDA UDI
Model / Reference
IPN044923 FDA UDI
Description
ET TUBE, EXCHANGER, ETX, 35 - 41 FR FDA UDI

Identifiers

Catalog Number
5-24105 FDA UDI
Primary DI / UDI-DI
04026704588626 FDA UDI
510(k) Number
K862347 FDA UDI
FDA Product Code
BTR FDA UDI
GMDN Term
Endotracheal tube guide, 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

No

FDA UDI

Dimensions & Sizes

Size
Length — 1000 Millimeter FDA UDI

Category: Endotracheal tube guide, single-use

Hudson Rci by Teleflex Incorporated — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Endotracheal tube guide, single-use.

Cleared under the same submission

K862347 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Teleflex Incorporated

Sources (1)

  • FDA UDI d45a4477-816e-4a79-bb3e-7197f5743665 38 fields · synced May 30, 2026