NAR Kit

FDA UDI

Class I (US FDA UDI)

by North American Rescue, Llc.

Identity

Trade Name: NAR Kit FDA UDI
Generic Name: Nasopharyngeal airway, single-use FDA UDI
Device Name: KIT, NASOPHARYNGEAL AIRWAY w' LUBE - 20F FDA UDI
Model / Reference: ZZ-1360 FDA UDI
Description: KIT, NASOPHARYNGEAL AIRWAY w' LUBE - 20F FDA UDI

Identifiers

Catalog Number: ZZ-1360 FDA UDI
Primary DI / UDI-DI: 00842209122349 FDA UDI
FDA Product Code: BTQ FDA UDI
OHO FDA UDI
GMDN Term: Nasopharyngeal airway, single-use FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 868.5100 FDA UDI
878.4014 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Dimensions & Sizes

Size: Catheter Gauge — 28 French FDA UDI

Category: First aid kit, non-medicated, single-use Nasopharyngeal airway, single-use General-body orifice lubricant

The NAR Kit is a single-use, rubber or plastic tube used to maintain airway patency in the nasopharynx. This device facilitates entry of diagnostic or therapeutic devices into the body orifice, reducing friction and facilitating its passage.

Similar devices

Also classified as General-body orifice lubricant.

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HR Lubricating Jelly — H R Pharmaceuticals, 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: North American Rescue, Llc.

Sources (1)

FDA UDI 2955ed66-027a-4de3-b377-484bd34b0cd4 35 fields · synced Jun 26, 2026