Hudson Rci

FDA UDI

Class II (US FDA UDI)

by Teleflex Incorporated

Identity

Trade Name: HUDSON RCI FDA UDI
Generic Name: Endobronchial tube FDA UDI
Device Name: ET TUBE, SHER-I-BRONCH, RS, 41 FR FDA UDI
Model / Reference: IPN048993 FDA UDI
Description: ET TUBE, SHER-I-BRONCH, RS, 41 FR FDA UDI

Identifiers

Catalog Number: 5-16141 FDA UDI
Primary DI / UDI-DI: 14026704617477 FDA UDI
510(k) Number: K851856 FDA UDI
FDA Product Code: CBI FDA UDI
GMDN Term: Endobronchial tube FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 868.5740 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

MRI Safety

MR Unsafe FDA UDI

Category: Endobronchial tube

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

Similar devices

Also classified as Endobronchial tube.

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Endobronchial Tube — Well Lead Medical Co., Ltd · Class II
SILBRONCHO (RIGHT LUNG) — Fuji Systems Corp. · Class II
UNIVENT TUBE (TCB TYPE) — Fuji Systems Corp. · Class II
Medline — MEDLINE INDUSTRIES, INC. · Class II

Cleared under the same submission

K851856 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Teleflex Incorporated

Sources (1)

FDA UDI 4f570d73-9ccb-48a1-b30d-870a5d8d4d3f 38 fields · synced May 30, 2026