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Disposable Conical Cuff

FDA UDI

Class I (US FDA UDI)

by Zhejiang Longyou Lande Medical Technology Co., Ltd.

Identity

Trade Name
Disposable Conical Cuff FDA UDI
Generic Name
Tourniquet cuff, single-use FDA UDI
Device Name
A pneumatic tourniquet is an air-powered device consisting of a pressure-regulating unit, connecting tubing, and an inflatable cuff. The cuff is intended to be wrapped around a patient's limb and inflated to reduce or totally occlude circulation during surgery. FDA UDI
Model / Reference
34"×4.3"; 100-8610 FDA UDI
Description
A pneumatic tourniquet is an air-powered device consisting of a pressure-regulating unit, connecting tubing, and an inflatable cuff. The cuff is intended to be wrapped around a patient's limb and inflated to reduce or totally occlude circulation during surgery. FDA UDI

Identifiers

Primary DI / UDI-DI
06976514770781 FDA UDI
FDA Product Code
KCY FDA UDI
GMDN Term
Tourniquet cuff, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.5910 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

Yes

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

Category: Tourniquet cuff, single-use

Disposable Conical Cuff by Zhejiang Longyou Lande Medical Technology Co., Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Tourniquet cuff, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 82151de2-1a19-4a9d-8dd0-7506205ee08b 33 fields · synced May 30, 2026