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Disposable Blood Pressure Cuff

EUDAMEDFDA UDI

Class I (EU MDR)

Ref V1023CModel philips IntelliVue and Avalon, Drage Vista 120, GE CARESCAPE™ B850 , etc

by Vistar Medical Supplies Co., Ltd.

Identity

Trade Name
Disposable Blood Pressure Cuff EUDAMED
Vistarmed FDA UDI
Generic Name
Blood pressure cuff, single-use FDA UDI
Device Name
Disposable Blood Pressure Cuff EUDAMED
Disposable NIBP cuff,Small adult,double tube, no connector FDA UDI
Model / Reference
philips IntelliVue and Avalon, Drage Vista 120, GE CARESCAPE™ B850 , etc EUDAMED
V1023C EUDAMEDFDA UDI
Description
Disposable NIBP cuff,Small adult,double tube, no connector FDA UDI

Identifiers

Primary DI / UDI-DI
96973521877260 EUDAMEDFDA UDI
Basic UDI-DI
697352187DBPCLH EUDAMED
510(k) Number
K152465 FDA UDI
FDA Product Code
DXQ FDA UDI
EMDN Code
Z1203020599 NON-INVASIVE BLOOD PRESSURE GAUGES - OTHER EUDAMED
GMDN Term
Blood pressure cuff, single-use FDA UDI

Classification

Device Class
Class I EUDAMED
Class II FDA UDI
Regulation Number
870.1120 FDA UDI
Market of Registration
Austria EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

Yes

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

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

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Disposable Blood Pressure Cuff by Vistar Medical Supplies Co., Ltd. — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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

Manufacturer

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

Sources (2)

  • EUDAMED 5b13b6b8-72ac-4160-93bb-0b7e5eac05f8 61 fields · synced Aug 3, 2026
  • FDA UDI 5e5506ab-f7fe-40fd-8566-23ffd8945662 34 fields · synced May 30, 2026