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BIOS Diagnostics

FDA UDI

Class II (US FDA UDI)

by Thermor Ltd

Identity

Trade Name
BIOS Diagnostics FDA UDI
Generic Name
Automatic-inflation electronic sphygmomanometer, portable, arm/wrist FDA UDI
Device Name
Blood Pressure Monitor/Automatic AFIB FDA UDI
Model / Reference
BD410 FDA UDI
Description
Blood Pressure Monitor/Automatic AFIB FDA UDI

Identifiers

Primary DI / UDI-DI
00057475244101 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

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

No

FDA UDI

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

BIOS Diagnostics by Thermor 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.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Thermor Ltd

Sources (1)

  • FDA UDI 494e4d1d-755e-46d1-926c-eacaaf47e9b5 33 fields · synced Jun 8, 2026