Rusch

FDA UDI

Class I (US FDA UDI)

by Teleflex Incorporated

Identity

Trade Name: RUSCH FDA UDI
Generic Name: Rigid optical laryngopharyngoscope FDA UDI
Device Name: SNAPLIGHT SET:GREENLED MEDIUM HANDLE+MAC 1,2,3,4 FDA UDI
Model / Reference: IPN915507 FDA UDI
Description: SNAPLIGHT SET:GREENLED MEDIUM HANDLE+MAC 1,2,3,4 FDA UDI

Identifiers

Catalog Number: 4261/L FDA UDI
Primary DI / UDI-DI: 14026704711878 FDA UDI
FDA Product Code: CCW FDA UDI
GMDN Term: Rigid optical laryngopharyngoscope FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 868.5540 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Sterilization Method

High-level Disinfectant FDA UDI

MRI Safety

MR Unsafe FDA UDI

Category: Rigid optical laryngopharyngoscope

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

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HOPKINS — Karl Storz GmbH & Co. KG · Class II
GlideScope® — Verathon Medical (Canada) ULC · Class I
GlideScope® — Verathon Medical (Canada) ULC · Class I
Millennium — AVALIGN TECHNOLOGIES, Inc. · Class I

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 I	Pending data

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Manufacturer

Manufacturer: Teleflex Incorporated

Sources (1)

FDA UDI 87bb54dd-c0f3-49fe-b28c-6a9555f605e3 35 fields · synced Jun 8, 2026