← Back to catalogue

BIA Electrodes

FDA UDI

Class II (US FDA UDI)

by R.j.l. Sciences, Inc.

Identity

Trade Name
BIA Electrodes FDA UDI
Generic Name
Electrocardiographic electrode, single-use FDA UDI
Device Name
Package contains 100 adhesive electrodes, sufficient for performing 25 BIA tests for whole-body body composition analysis. FDA UDI
Model / Reference
92500 FDA UDI
Description
Package contains 100 adhesive electrodes, sufficient for performing 25 BIA tests for whole-body body composition analysis. FDA UDI

Identifiers

Catalog Number
92500P FDA UDI
Primary DI / UDI-DI
B202925001 FDA UDI
FDA Product Code
DRX FDA UDI
GMDN Term
Electrocardiographic electrode, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.2360 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

Yes

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Electrocardiographic electrode, single-use

BIA Electrodes by R.j.l. Sciences, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electrocardiographic electrode, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
R.j.l. Sciences, Inc.

Sources (1)

  • FDA UDI cc3a5c9c-b344-41de-8d9b-fb51fedf6cfd 35 fields · synced May 30, 2026