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MedSource Airway Devices

FDA UDI

Class I (US FDA UDI)

by Medsource International Llc

Identity

Trade Name
MedSource Airway Devices FDA UDI
Generic Name
Nasopharyngeal airway, single-use FDA UDI
Device Name
Robertazzi Naso Airway, 32fr FDA UDI
Model / Reference
MS-23962 FDA UDI
Description
Robertazzi Naso Airway, 32fr FDA UDI

Identifiers

Catalog Number
Not Applicable FDA UDI
Primary DI / UDI-DI
00816703026724 FDA UDI
FDA Product Code
BTQ FDA UDI
GMDN Term
Nasopharyngeal airway, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5100 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

No

FDA UDI

Category: Nasopharyngeal airway, single-use

MedSource Airway Devices by Medsource International Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Nasopharyngeal airway, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI de4d4fe3-6f64-4d47-b89f-d927701b483a 34 fields · synced Jun 8, 2026