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Biovitals Analytics Engine

FDA UDI

Class II (US FDA UDI)

by Biofourmis Singapore Pte., Ltd.

Identity

Trade Name
Biovitals Analytics Engine FDA UDI
Generic Name
Physiologic monitor-installed software FDA UDI
Model / Reference
2.0 FDA UDI

Identifiers

Primary DI / UDI-DI
08885018690021 FDA UDI
510(k) Number
K183282 FDA UDI
FDA Product Code
PLB FDA UDI
GMDN Term
Physiologic monitor-installed software FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.2300 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: Physiologic monitor-installed software

Biovitals Analytics Engine by Biofourmis Singapore Pte., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Physiologic monitor-installed software.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 7aceb156-be10-468f-b7cd-756e478a0d0d 33 fields · synced May 30, 2026