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Nar

FDA UDI

Class I (US FDA UDI)

by North American Rescue, Llc.

Identity

Trade Name
NAR FDA UDI
Generic Name
Arterial tourniquet, manual, single-use FDA UDI
Model / Reference
85-2005 FDA UDI

Identifiers

Catalog Number
85-2005 FDA UDI
Primary DI / UDI-DI
00842209119349 FDA UDI
FDA Product Code
GAX FDA UDI
GMDN Term
Arterial tourniquet, manual, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.5900 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

No

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Arterial tourniquet, manual, single-use

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

Similar devices

Also classified as Arterial tourniquet, manual, single-use.

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 0d064484-c32b-4fb3-bb48-643e92280372 33 fields · synced May 30, 2026