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Rusch

FDA UDI

Class II (US FDA UDI)

by Teleflex Incorporated

Identity

Trade Name
RUSCH FDA UDI
Generic Name
Laryngectomy tube FDA UDI
Device Name
Laryngectomy tube, cuffed FDA UDI
Model / Reference
IPN041900 FDA UDI
Description
Laryngectomy tube, cuffed FDA UDI

Identifiers

Catalog Number
121181-000090 FDA UDI
Primary DI / UDI-DI
04026704012923 FDA UDI
FDA Product Code
BTO FDA UDI
GMDN Term
Laryngectomy tube FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5800 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

Yes

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 — 9 Millimeter FDA UDI
Outer Diameter — 12.4 Millimeter FDA UDI

Category: Laryngectomy tube

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

Similar devices

Also classified as Laryngectomy tube.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 77eb7848-c05d-4b18-8729-4e4bc61cbd4a 36 fields · synced Jun 8, 2026