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Compressible Limb Therapy System

FDA UDI

Class II (US FDA UDI)

by Daesung Maref Co., Ltd.

Identity

Trade Name
Compressible Limb Therapy System FDA UDI
Generic Name
Pneumatic massager FDA UDI
Device Name
Sequential compression pump (pump only) FDA UDI
Model / Reference
LX7(V7) FDA UDI
Description
Sequential compression pump (pump only) FDA UDI

Identifiers

Primary DI / UDI-DI
08809315677806 FDA UDI
510(k) Number
K102320 FDA UDI
FDA Product Code
IRP FDA UDI
GMDN Term
Pneumatic massager FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
890.5650 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

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Pneumatic massager

Compressible Limb Therapy System by Daesung Maref Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Pneumatic massager.

Cleared under the same submission

K102320 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Daesung Maref Co., Ltd.

Sources (1)

  • FDA UDI 3559169f-ff98-444f-bf49-f513149ecb2b 34 fields · synced May 30, 2026