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Rusch

FDA UDI

Class II (US FDA UDI)

by Teleflex Incorporated

Identity

Trade Name
RUSCH FDA UDI
Generic Name
Tracheostomy kit, single-use FDA UDI
Device Name
PERCUQUICK PDT, STERILE FDA UDI
Model / Reference
IPN042004 FDA UDI
Description
PERCUQUICK PDT, STERILE FDA UDI

Identifiers

Catalog Number
121550-000090 FDA UDI
Primary DI / UDI-DI
04026704094110 FDA UDI
FDA Product Code
JOH FDA UDI
GMDN Term
Tracheostomy kit, single-use 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

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
Length — 190 Millimeter FDA UDI
Outer Diameter — 12.7 Millimeter FDA UDI

Category: Tracheostomy kit, single-use

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

Similar devices

Also classified as Tracheostomy kit, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Teleflex Incorporated

Sources (1)

  • FDA UDI 57e98919-a7ed-4db5-9da0-185a9790f552 36 fields · synced May 30, 2026