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DVT Garment

by Vistar Medical Supplies Co., Ltd. 24 variants

Ref DVT10F12Model Cardinalhealth:Kendall SCD™ 700 Series, Longest:LGT-2201DVT, etc.

Active European Union. Also listed in GUDID (US).

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

None found

in data synced 25 Oct 2026

Documents

None, self-declared

Class I: no certifier involved

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, GUDID, synced 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing GUDID Number96973521878595 UDI-DI Date22 Jul 2026ListedStatusListed GUDID: in commercial distribution
European UnionCE/MDR EUDAMED Number6973521878DVT9HF Basic UDI-DI 96973521878595UDI-DIDate5 Dec 2025RegisteredStatusActive

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 25 Oct 2026.

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDR Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Trade Name
DVT Garment EUDAMED
BlissCuff GUDID
Generic Name
Multi-chamber venous compression system garment, single-use
Model / Reference
Cardinalhealth:Kendall SCD™ 700 Series, Longest:LGT-2201DVT, etc., DVT10F12
Primary DI / UDI-DI
96973521878595
Basic UDI-DI
6973521878DVT9HF
510(k) Number
FDA Product Code
JOW
EMDN Code
Z12069099 Various physiotherapy and rehabilitation instruments - other
GMDN Term
Multi-chamber venous compression system garment, single-use
Device Class
Class I EUDAMED
Class II GUDID
Regulation Number
870.5800
EU market of registration
Austria
GUDID distribution status
In Commercial Distribution
MRI Safety
MR Unsafe

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device ClassEUDAMED
Class I
GUDID
Class II

Manufacturer details

EUDAMED SRN
CN-MF-000011207
Authorised representative
RIOMAVIX SOCIEDAD LIMITADA ES-AR-000001202

Other devices from Vistar Medical Supplies Co., Ltd.

See all devices from Vistar Medical Supplies Co., Ltd. →

Properties

  • Single Use
  • Expiration Date
  • Manufacturing Date

Other properties (21)

  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No
  • Prescription Use: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Lot / Batch Number: No
  • Serial Number: No