Nar

FDA UDI

Class I (US FDA UDI)

by North American Rescue, Llc.

Identity

Trade Name: NAR FDA UDI
Generic Name: Conduction blood/fluid warmer FDA UDI
Device Name: KIT, QUANTUM ULTIMATE INTENSIVE RESUSCITATION CARRY (Q.U.I.C.K.) - BASIC FDA UDI
Model / Reference: 35-0026 FDA UDI
Description: KIT, QUANTUM ULTIMATE INTENSIVE RESUSCITATION CARRY (Q.U.I.C.K.) - BASIC FDA UDI

Identifiers

Catalog Number: 35-0026 FDA UDI
Primary DI / UDI-DI: 00842209125159 FDA UDI
FDA Product Code: OHO FDA UDI
LGZ FDA UDI
BSB FDA UDI
GMDN Term: Conduction blood/fluid warmer FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 878.4014 FDA UDI
880.5725 FDA UDI
864.9205 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

MRI Safety

MR Unsafe FDA UDI

Category: First aid kit, non-medicated, single-use Conduction blood/fluid warmer

Nar by North American Rescue, Llc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Conduction blood/fluid warmer.

Ranger™ — 3M COMPANY · Class II
ThermaCor 1200 Infusion System — Smisson-Cartledge Biomedical, LLC · Class II
Curaplex — BOUND TREE MEDICAL, LLC · Class II
ASTOLINE — Stihler Electronic GmbH · Class II
ASTOTHERM® PLUS — Stihler Electronic GmbH · Class II
EXPRESS FLUID WARMER — NxStage Medical, Inc. · Class II
°M Warmer System - Charger — Mequ A/S · Class II
ASTOFLO® PLUS ECO — Stihler Electronic GmbH · Class II

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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer: North American Rescue, Llc.

Sources (1)

FDA UDI 4a5ff589-9299-4517-8aa5-0619ddcd254f 34 fields · synced May 30, 2026