← Back to catalogue

Dvt3200

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref DVT3200Model DVT-2600

by Daesung Maref Co., Ltd.

Identity

Trade Name
DVT-2600 FDA UDI
Generic Name
Sequential venous compression system inflator FDA UDI
Device Name
DVT-2600 Device 1ea FDA UDI
Model / Reference
DVT-2600 EUDAMED
DVT3200 EUDAMEDFDA UDI
Description
DVT-2600 Device 1ea FDA UDI

Identifiers

Primary DI / UDI-DI
08809315675307 EUDAMEDFDA UDI
Basic UDI-DI
B-08809315675307 EUDAMED
510(k) Number
K203016 FDA UDI
FDA Product Code
JOW FDA UDI
EMDN Code
Z120607 PNEUMATIC COMPRESSION EQUIPMENT EUDAMED
GMDN Term
Sequential venous compression system inflator FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class II FDA UDI
Regulation Number
870.5800 FDA UDI
Market of Registration
France EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

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

Dvt3200 by Daesung Maref Co., Ltd. — Class IIa — MDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDD

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
KR-MF-000008616
Authorised Representative
KTR Europe GmbH DE-AR-000005685

Sources (2)

  • EUDAMED 51774513-de34-4c79-bcab-be953bb1bc64 61 fields · synced Jul 9, 2026
  • FDA UDI 516ebe3f-8831-41db-acd2-1ae82db3c3a0 34 fields · synced May 30, 2026