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Junctional Emergency Treatment Tool (jett®)

FDA UDI

Class II (US FDA UDI)

by North American Rescue, Llc.

Identity

Trade Name
JUNCTIONAL EMERGENCY TREATMENT TOOL (JETT®) FDA UDI
Generic Name
Emergency junctional haemorrhage compression set FDA UDI
Device Name
JUNCTIONAL EMERGENCY TREATMENT TOOL (JETT®) For treating high extremity wounds in the thigh/groin region at or near point of injury, includes two pressure devices in a single tool, allowing for simultaneous occlusion of blood flow to both lower limbs (bilateral) with an easy to apply, pre-assembled, ready-to-use belt solution Single use. FDA UDI
Model / Reference
30-0088 FDA UDI
Description
JUNCTIONAL EMERGENCY TREATMENT TOOL (JETT®) For treating high extremity wounds in the thigh/groin region at or near point of injury, includes two pressure devices in a single tool, allowing for simultaneous occlusion of blood flow to both lower limbs (bilateral) with an easy to apply, pre-assembled, ready-to-use belt solution Single use. FDA UDI

Identifiers

Catalog Number
30-0088 FDA UDI
Primary DI / UDI-DI
00842209100002 FDA UDI
510(k) Number
K123194 FDA UDI
FDA Product Code
DXC FDA UDI
GMDN Term
Emergency junctional haemorrhage compression set FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.4450 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Emergency junctional haemorrhage compression set

Junctional Emergency Treatment Tool (jett®) by North American Rescue, Llc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Emergency junctional haemorrhage compression set.

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 761754ea-20a2-4409-b24b-e768911b3633 35 fields · synced Jun 1, 2026