Rusch

FDA UDI

Class II (US FDA UDI)

by Teleflex Incorporated

Identity

Trade Name: RUSCH FDA UDI
Generic Name: Basic endotracheal tube, single-use FDA UDI
Device Name: PREFORMED AGT NASAL ENDOTRACHEAL TUBE - MURPHY EYE, HIGH VOLUME, LOW PRESSURE CUFF - STERILE PACK FDA UDI
Model / Reference: IPN041445 FDA UDI
Description: PREFORMED AGT NASAL ENDOTRACHEAL TUBE - MURPHY EYE, HIGH VOLUME, LOW PRESSURE CUFF - STERILE PACK FDA UDI

Identifiers

Catalog Number: 111781055 FDA UDI
Primary DI / UDI-DI: 14026704341198 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

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

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

Yes

FDA UDI

Dimensions & Sizes

Size: Width — 25 Millimeter FDA UDI
Height — 16.5 Millimeter FDA UDI
Length — 325 Millimeter FDA UDI
Outer Diameter — 7.3 Millimeter FDA UDI

Category: Basic endotracheal tube, single-use

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

Similar devices

Also classified as Basic endotracheal tube, single-use.

AVANOS — Avanos Medical, Inc. · Class II
Parker Flex-Tip — SALTER LABS · Class II
Mallinckrodt — Covidien LP · Class II
RediTube™ — Airlife, Inc. · Class II
Medline Industries, Inc. — MEDLINE INDUSTRIES, INC. · Class II
Endotracheal Tubes — Dynarex Corp. · Class II
ULTRAMED ENDOTRACHEAL TUBE ORAL/NASAL CUFFED Size 3 — Ultra For Medical Products (Ultramed) U.M.I.C (S.A.E) · Class IIa
Rurka intubacyjna z mankietem — SUMI spółka z ograniczoną odpowiedzialnością spółka komandytowa · Class IIa

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

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

Manufacturer

Manufacturer: Teleflex Incorporated

Sources (1)

FDA UDI f858dd90-5db8-4c63-9ac8-fab121caa750 35 fields · synced May 30, 2026