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Vitaltrack

FDA UDI

Class II (US FDA UDI)

by Shenzhen Urion Technology Co., Ltd.

Identity

Trade Name
VITALTRACK FDA UDI
Generic Name
Automatic-inflation electronic sphygmomanometer, portable, arm/wrist FDA UDI
Device Name
N/A FDA UDI
Model / Reference
U80EH FDA UDI
Description
N/A FDA UDI

Identifiers

Catalog Number
Yes FDA UDI
Primary DI / UDI-DI
06953825906962 FDA UDI
510(k) Number
K243115 FDA UDI
FDA Product Code
DXN FDA UDI
GMDN Term
Automatic-inflation electronic sphygmomanometer, portable, arm/wrist FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1130 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

Yes

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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Automatic-inflation electronic sphygmomanometer, portable, arm/wrist

Vitaltrack by Shenzhen Urion Technology Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Automatic-inflation electronic sphygmomanometer, portable, arm/wrist.

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 54a725ff-33af-4abb-afaf-3b0415380161 35 fields · synced Jun 8, 2026