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Dvt-Series

FDA UDI

Class II (US FDA UDI)

by Daesung Maref Co., Ltd.

Identity

Trade Name
DVT-SERIES FDA UDI
Generic Name
Multi-chamber venous compression system garment, reusable FDA UDI
Device Name
MULTI-USE CALF SLEEVE, Medium, 2ea [One polybag] FDA UDI
Model / Reference
DS121 FDA UDI
Description
MULTI-USE CALF SLEEVE, Medium, 2ea [One polybag] FDA UDI

Identifiers

Primary DI / UDI-DI
08809315675369 FDA UDI
510(k) Number
K203016 FDA UDI
K203417 FDA UDI
FDA Product Code
JOW FDA UDI
GMDN Term
Multi-chamber venous compression system garment, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.5800 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

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

Yes

FDA UDI

Category: Multi-chamber venous compression system garment, reusable

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

Similar devices

Also classified as Multi-chamber venous compression system garment, reusable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI c9846ce8-59b6-4017-9736-9178f5cc2fe1 34 fields · synced Jun 8, 2026