← Back to catalogue

Smart Trace Electrodes .080 in

FDA UDI

Class II (US FDA UDI)

by Circadiance

Identity

Trade Name
Smart Trace Electrodes .080 in FDA UDI
Generic Name
Neonatal electrocardiographic electrode FDA UDI
Device Name
Smart Trace Electrodes .080 in., 20 Pairs FDA UDI
Model / Reference
1015662 FDA UDI
Description
Smart Trace Electrodes .080 in., 20 Pairs FDA UDI

Identifiers

Catalog Number
1015662 FDA UDI
Primary DI / UDI-DI
B0361015662 FDA UDI
510(k) Number
K000206 FDA UDI
FDA Product Code
DRX FDA UDI
GMDN Term
Neonatal electrocardiographic electrode 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

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Neonatal electrocardiographic electrode

Smart Trace Electrodes .080 in by Circadiance — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Neonatal electrocardiographic electrode.

Cleared under the same submission

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
Circadiance

Sources (1)

  • FDA UDI 0a344b14-2ab7-4438-8a88-2fefdb2e214a 37 fields · synced Jun 9, 2026