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Rusch

FDA UDI

Class II (US FDA UDI)

by Teleflex Incorporated

Identity

Trade Name
RUSCH FDA UDI
Generic Name
Basic endotracheal tube, reusable FDA UDI
Device Name
Tracheal tube, cuffed FDA UDI
Model / Reference
IPN040871 FDA UDI
Description
Tracheal tube, cuffed FDA UDI

Identifiers

Catalog Number
102000-000095 FDA UDI
Primary DI / UDI-DI
04026704002108 FDA UDI
FDA Product Code
BTR FDA UDI
GMDN Term
Basic endotracheal tube, reusable 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

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

Yes

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
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size
Lumen/Inner Diameter — 9.5 Millimeter FDA UDI

Category: Basic endotracheal tube, reusable

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

Similar devices

Also classified as Basic endotracheal tube, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Teleflex Incorporated

Sources (1)

  • FDA UDI 92502e00-521a-4cf3-b217-49314f5f14f9 36 fields · synced May 30, 2026