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Rusch

FDA UDI

Class I (US FDA UDI)

by Teleflex Incorporated

Identity

Trade Name
RUSCH FDA UDI
Generic Name
Laryngoscope handle, single-use FDA UDI
Device Name
RUSCH® Polaris™ STUBBY FIBER OPTIC DISPOSABLE LARYNGOSCOPE HANDLE WITH BATTERIES FDA UDI
Model / Reference
IPN039531 FDA UDI
Description
RUSCH® Polaris™ STUBBY FIBER OPTIC DISPOSABLE LARYNGOSCOPE HANDLE WITH BATTERIES FDA UDI

Identifiers

Catalog Number
44403 FDA UDI
Primary DI / UDI-DI
14026704662576 FDA UDI
FDA Product Code
CCW FDA UDI
GMDN Term
Laryngoscope handle, single-use 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

No

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

Category: Laryngoscope handle, single-use

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

Similar devices

Also classified as Laryngoscope handle, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI deeb1dd2-d7c2-49a9-913c-2b7420ab9fa2 35 fields · synced May 30, 2026