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Bothealth

FDA UDIEUDAMED

Class II (US FDA UDI)

by Shenzhen BSX Technology Electronics Co., Ltd.

Identity

Trade Name
BOTHEALTH FDA UDI
Generic Name
Patient monitoring system module, blood pressure, noninvasive FDA UDI
Model / Reference
BSX525 FDA UDI

Identifiers

Primary DI / UDI-DI
06920485305251 FDA UDI
510(k) Number
K183058 FDA UDI
FDA Product Code
DXN FDA UDI
GMDN Term
Patient monitoring system module, blood pressure, noninvasive 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

Yes

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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Patient monitoring system module, blood pressure, noninvasive

Bothealth by Shenzhen BSX Technology Electronics Co., Ltd. — Class II — MDD, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Patient monitoring system module, blood pressure, noninvasive.

Cleared under the same submission

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDD

United States Pending data

FDA UDI

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Manufacturer

Sources (2)

  • FDA UDI ba6d292a-1f2d-4d68-8ea8-871de0048771 33 fields · synced Jun 1, 2026
  • EUDAMED 1 fields · synced May 22, 2026