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FORWARD AAJT-S Deployment Kit

FDA UDI

Class II (US FDA UDI)

by Integrated Medcraft Llc

Identity

Trade Name
FORWARD AAJT-S Deployment Kit FDA UDI
Generic Name
Emergency junctional haemorrhage compression set FDA UDI
Device Name
FORWARD AAJT-S Deployment Kit includes AAJT-S Junctional Tourniquet and Carry Pouch. FDA UDI
Model / Reference
1101-22000CB FDA UDI
Description
FORWARD AAJT-S Deployment Kit includes AAJT-S Junctional Tourniquet and Carry Pouch. FDA UDI

Identifiers

Primary DI / UDI-DI
00850056748001 FDA UDI
510(k) Number
K221661 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

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: Emergency junctional haemorrhage compression set

FORWARD AAJT-S Deployment Kit by Integrated Medcraft 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
Integrated Medcraft Llc

Sources (1)

  • FDA UDI fc075330-9663-41d7-96b0-be09f6b4669e 34 fields · synced Jun 8, 2026