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Bindex Measure

FDA UDI

Class I (US FDA UDI)

by Bone Index Finland , Ltd.

Identity

Trade Name
Bindex Measure FDA UDI
Generic Name
Bone absorptiometric ultrasound system FDA UDI
Device Name
Measuring stick for defining the standard location for Bindex measurement. FDA UDI
Model / Reference
BI-41 FDA UDI
Description
Measuring stick for defining the standard location for Bindex measurement. FDA UDI

Identifiers

Primary DI / UDI-DI
06430065790020 FDA UDI
FDA Product Code
FTY FDA UDI
GMDN Term
Bone absorptiometric ultrasound system FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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

Yes

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Bone absorptiometric ultrasound system

Bindex Measure by Bone Index Finland , Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bone absorptiometric ultrasound system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Bone Index Finland , Ltd.

Sources (1)

  • FDA UDI 5883bf29-20df-4860-a5a4-e877d58973cb 34 fields · synced Jun 8, 2026