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Vistarmed V0111C-DM

by Shenzhen Vistar Medical Supplies Co., Ltd.

Part of a family of 208 devices: see the family page

Ref V0111C-DM

Vistarmed V0111C-DM is a device classified as Class I in the EU and Class II in the US made by Shenzhen Vistar Medical Supplies Co., Ltd., registered in EUDAMED on 5 Dec 2025 (Basic UDI-DI 697352187RBPCPK), cleared under FDA 510(k) K152468 on 29 Oct 2015 and listed in FDA GUDID since 10 Aug 2020 (UDI-DI 96973521874313), active as of 23 Oct 2026.

Active European Union and United States. Also listed in GUDID (US).

CE MDR 510(k)

Valid until

No date given

CE: no date in EUDAMED. FDA: not time-limited

FDA recalls

None found

in data synced 23 Oct 2026

Documents

None linked in EUDAMED

A group certificate may exist

510(k) K152468

FDA submission, from GUDID

Trust

Unverified

Source EUDAMED, GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number697352187RBPCPK Basic UDI-DI 96973521874313UDI-DIDate5 Dec 2025RegisteredStatusActive
United StatesGUDID listing GUDID Number96973521874313 UDI-DI Date10 Aug 2020ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE GUDID from GUDID Substantially Equivalent · Traditional NumberK152468 Date29 Oct 2015DecidedStatusActive

Official records

Across registries

3 registries list this device

  • EUDAMED Basic UDI-DI 697352187RBPCPK registered 5 Dec 2025 Active
  • FDA 510(k) K152468 decided 29 Oct 2015 Active
  • FDA GUDID UDI-DI 96973521874313 listed 10 Aug 2020 Listed

Timeline

3 dated events

  1. Cleared FDA 510(k) K152468
  2. Listed FDA GUDID 96973521874313
  3. Registered EUDAMED 697352187RBPCPK

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDR Active
  • United States FDA 510(k) Active

Specification

EUDAMED · GUDID

Trade name
Reusable Blood Pressure Cuff EUDAMED
Vistarmed GUDID
Generic name
Blood pressure cuff, reusable
Model / reference
V0111C-DM
Primary DI / UDI-DI
96973521874313
Basic UDI-DI
697352187RBPCPK
510(k) Number
FDA product code
DXQ
EMDN code
Z1203020599 Non-invasive blood pressure gauges - other
GMDN term
Blood pressure cuff, reusable
Device class
Class I EUDAMED
Class II GUDID
Regulation number
870.1120
EU registration type
Standard device
EU market of registration
Austria
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device classEUDAMED
Class I
GUDID
Class II

Device class is stated on each registry's own scale: Class I in the EU (EUDAMED), Class II in the US (FDA GUDID). EU and US classes are different schemes, so this is not a disagreement.

Related devices

Category: Blood pressure cuff, reusable

Cleared under the same submission (K152468)

and 8 more cleared under K152468

Similar devices in this category

Other devices filed under NON-INVASIVE BLOOD PRESSURE GAUGES - OTHER.

Other devices from Shenzhen Vistar Medical Supplies Co., Ltd.

  • Vistarmed V0014C-HPM

    Class II

  • Vistarmed V1011N-HP

    Class II

  • Vistarmed V1015N-HP

    Class II

  • Vistarmed V0126C-HP

    Class II

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

Properties

  • Reusable
  • Lot / batch number
  • Serial number
  • Expiration date
  • Manufacturing date
Other properties (20, all answered No)