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Rusch

FDA UDI

Class I (US FDA UDI)

by Teleflex Incorporated

Identity

Trade Name
RUSCH FDA UDI
Generic Name
Oropharyngeal airway, single-use FDA UDI
Device Name
Berman Airway 70mm ISO 7 FDA UDI
Model / Reference
IPN049397 FDA UDI
Description
Berman Airway 70mm ISO 7 FDA UDI

Identifiers

Catalog Number
122070 FDA UDI
Primary DI / UDI-DI
34026704624059 FDA UDI
FDA Product Code
CAE FDA UDI
GMDN Term
Oropharyngeal airway, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5110 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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Oropharyngeal airway, single-use

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

Similar devices

Also classified as Oropharyngeal airway, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI c466d546-7112-4bb7-9dce-8892174ba3c5 35 fields · synced Jun 8, 2026