← Back to catalogue

Rusch

FDA UDI

Class II (US FDA UDI)

by Teleflex Incorporated

Identity

Trade Name
RUSCH FDA UDI
Generic Name
Laser-resistant endotracheal tube FDA UDI
Device Name
Endotracheal tube for laser surgery FDA UDI
Model / Reference
IPN040899 FDA UDI
Description
Endotracheal tube for laser surgery FDA UDI

Identifiers

Catalog Number
102004-000060 FDA UDI
Primary DI / UDI-DI
04026704002665 FDA UDI
510(k) Number
K935842 FDA UDI
FDA Product Code
BTR FDA UDI
GMDN Term
Laser-resistant endotracheal tube 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

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size
Lumen/Inner Diameter — 6 Millimeter FDA UDI

Category: Laser-resistant endotracheal tube

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

Similar devices

Also classified as Laser-resistant endotracheal tube.

Cleared under the same submission

K935842 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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

Manufacturer

Manufacturer
Teleflex Incorporated

Sources (1)

  • FDA UDI ec482574-6dce-49ac-a758-8d2b696fefa2 38 fields · synced Jun 8, 2026