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Vistarmed

FDA UDI

Class II (US FDA UDI)

by Shenzhen Vistar Medical Supplies Co., Ltd.

Identity

Trade Name
Vistarmed FDA UDI
Generic Name
Blood pressure cuff, reusable FDA UDI
Device Name
Reusable NIBP cuff,Small adult,single tube, no connector FDA UDI
Model / Reference
V0113C FDA UDI
Description
Reusable NIBP cuff,Small adult,single tube, no connector FDA UDI

Identifiers

Primary DI / UDI-DI
96973521873965 FDA UDI
510(k) Number
K152468 FDA UDI
FDA Product Code
DXQ FDA UDI
GMDN Term
Blood pressure cuff, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1120 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

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

Category: Blood pressure cuff, reusable

Vistarmed by Shenzhen Vistar Medical Supplies Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Blood pressure cuff, reusable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 87df9ef0-48df-42f8-adec-191bbfe46041 34 fields · synced May 30, 2026