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Sterile Single-use Tourniquet Cuff

EUDAMEDFDA UDI

Class I (EU MDR)

Ref VTS-115

by Vistar Medical Supplies Co., Ltd.

Identity

Trade Name
Sterile Single-use Tourniquet Cuff EUDAMED
N/A FDA UDI
Generic Name
Tourniquet cuff, single-use FDA UDI
Device Name
Sterile Single-use Tourniquet Cuff EUDAMED
STERILE DISPOSABLE TOURNIQUET CUFF,SINGLE PORT, SINGLE BLADDER, 24 IN FDA UDI
Model / Reference
VTS-115 EUDAMED
VT-115 FDA UDI
Description
STERILE DISPOSABLE TOURNIQUET CUFF,SINGLE PORT, SINGLE BLADDER, 24 IN FDA UDI

Identifiers

Primary DI / UDI-DI
96973521872456 EUDAMEDFDA UDI
Basic UDI-DI
697352187DSTQSRG EUDAMED
FDA Product Code
KCY FDA UDI
EMDN Code
Z12139006 PNEUMATIC TOURNIQUETS EUDAMED
GMDN Term
Tourniquet cuff, single-use FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
878.5910 FDA UDI
Market of Registration
Austria EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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

No

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size
Length — 24 Inch FDA UDI

Category: Tourniquet cuff, single-use

Sterile Single-use Tourniquet Cuff by Vistar Medical Supplies Co., Ltd. — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Tourniquet cuff, single-use.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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Manufacturer

EUDAMED SRN
CN-MF-000011207
Authorised Representative
RIOMAVIX SOCIEDAD LIMITADA ES-AR-000001202

Sources (2)

  • EUDAMED afed0fe0-282f-44e1-8efd-21bac26cf7e4 61 fields · synced Jul 14, 2026
  • FDA UDI eecd8a62-d07d-4254-bec6-7ff508157dee 34 fields · synced May 30, 2026