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Disposable Blood Pressure Cuff

by Vistar Medical Supplies Co., Ltd. 62 variants

Ref V1015CModel philips IntelliVue and Avalon, Drage Vista 120, GE CARESCAPE™ B850 , 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 24 Oct 2026

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, GUDID, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number697352187DBPCLH Basic UDI-DI Date4 Dec 2025RegisteredStatusActive
United StatesGUDID listing GUDID Number96973521877192 UDI-DI Date29 Jul 2020ListedStatusListed GUDID: in commercial distribution

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 24 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  • Withdrawn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
Disposable Blood Pressure Cuff EUDAMED
Vistarmed GUDID
Generic Name
Blood pressure cuff, single-use
Device Name
Reusable Blood Pressure Cuff
Model / Reference
philips IntelliVue and Avalon, Drage Vista 120, GE CARESCAPE™ B850, etc, V1015C
Primary DI / UDI-DI
96973521877192, 96973521870759
Basic UDI-DI
697352187DBPCLH, 697352187RBPCPK
510(k) Number
FDA Product Code
DXQ
EMDN Code
Z1203020599 Non-invasive blood pressure gauges - other
GMDN Term
Blood pressure cuff, single-use
Device Class
Class I EUDAMED
Class II GUDID
Regulation Number
870.1120
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

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
  • Reusable NoEUDAMEDYesEUDAMED
  • Lot / Batch Number
  • Serial Number
  • Expiration Date
  • Manufacturing Date

Other properties (18)

  • Sterile: No
  • Implantable: 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