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SAM® Junctional Tourniquet

EUDAMEDFDA UDI

Class I (EU MDR)

Ref JT400-EN

by SAM Medical Products

Identity

Trade Name
SAM® Junctional Tourniquet EUDAMEDFDA UDI
Generic Name
Emergency junctional haemorrhage compression set FDA UDI
Device Name
SAM® Junctional Tourniquet EUDAMED
SAM Junctional Tourniquet - SJT Belt with 2 TCDs, Auxiliary Strap, Extender, Hand Pump & Bag FDA UDI
Model / Reference
JT400-EN EUDAMEDFDA UDI
Description
SAM Junctional Tourniquet - SJT Belt with 2 TCDs, Auxiliary Strap, Extender, Hand Pump & Bag FDA UDI

Identifiers

Primary DI / UDI-DI
00822045000353 EUDAMEDFDA UDI
Basic UDI-DI
0822045JT01TF EUDAMED
510(k) Number
K131561 FDA UDI
FDA Product Code
DXC FDA UDI
EMDN Code
V9003 TOURNIQUETS EUDAMED
GMDN Term
Emergency junctional haemorrhage compression set FDA UDI

Classification

Device Class
Class I EUDAMED
Class II FDA UDI
Regulation Number
870.4450 FDA UDI
Market of Registration
Netherlands EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

Yes

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

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

No

FDA UDI

Category: Limb tourniquet, manual, reusable

SAM® Junctional Tourniquet by SAM Medical Products — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Limb tourniquet, manual, reusable.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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Manufacturer

EUDAMED SRN
US-MF-000002589
Authorised Representative
Emergo Europe B.V. NL-AR-000000116

Sources (2)

  • EUDAMED b6d04416-7646-4fd4-aaa0-d1b8201df947 61 fields · synced Jun 8, 2026
  • FDA UDI 9ee59c84-df5c-480c-a72d-2ac44d1b8e30 35 fields · synced May 30, 2026