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Nar

FDA UDI

Class II (US FDA UDI)

by North American Rescue, Llc.

Identity

Trade Name
NAR FDA UDI
Generic Name
Blood transfusion set, non-exchange FDA UDI
Device Name
KIT, FBTK RECIPIENT MODULE FDA UDI
Model / Reference
83-0002 FDA UDI
Description
KIT, FBTK RECIPIENT MODULE FDA UDI

Identifiers

Catalog Number
83-0002 FDA UDI
Primary DI / UDI-DI
00842209103737 FDA UDI
FDA Product Code
POQ FDA UDI
GMDN Term
Blood transfusion set, non-exchange FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5440 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

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Blood transfusion set, non-exchange

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

Similar devices

Also classified as Blood transfusion set, non-exchange.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
North American Rescue, Llc.

Sources (1)

  • FDA UDI cb26e0e1-657d-4941-992b-461b04354038 34 fields · synced May 31, 2026