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Lf900

FDA UDI

Class II (US FDA UDI)

by Daesung Maref Co., Ltd.

Identity

Trade Name
LF900 FDA UDI
Generic Name
Intermittent venous compression system FDA UDI
Device Name
Main device 1ea, LEG SLEEVE XLarge 2ea, Double Hose 1ea, Recovery Bag 1ea [One set box] FDA UDI
Model / Reference
LF90200-RX FDA UDI
Description
Main device 1ea, LEG SLEEVE XLarge 2ea, Double Hose 1ea, Recovery Bag 1ea [One set box] FDA UDI

Identifiers

Primary DI / UDI-DI
08809315677004 FDA UDI
510(k) Number
K203019 FDA UDI
FDA Product Code
IRP FDA UDI
GMDN Term
Intermittent venous compression system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
890.5650 FDA UDI
Commercial Distribution
Not 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

Lf900 by Daesung Maref Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Cleared under the same submission

K203019 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 a5db807c-9da2-431c-9550-0a0bceab4647 35 fields · synced May 31, 2026