QuickScan Pads & Electrodes Pack

FDA UDI

Class I (US FDA UDI)

by Precision Biometrics Inc

Identity

Trade Name: QuickScan Pads & Electrodes Pack FDA UDI
Generic Name: Electrode conductive medium FDA UDI
Device Name: 3 pack of Single Jar pads, 00853818007156 3 packs of 10ea static electrodes (PB-212), 00853818007231 1 Medical Tweezer, 00853818007170 FDA UDI
Model / Reference: PB-35 FDA UDI
Description: 3 pack of Single Jar pads, 00853818007156 3 packs of 10ea static electrodes (PB-212), 00853818007231 1 Medical Tweezer, 00853818007170 FDA UDI

Identifiers

Primary DI / UDI-DI: 00853818007255 FDA UDI
FDA Product Code: KQX FDA UDI
HCS FDA UDI
HCC FDA UDI
IKN FDA UDI
GMDN Term: Electrode conductive medium FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 888.1500 FDA UDI
882.1570 FDA UDI
882.5050 FDA UDI
890.1375 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: Electrocardiographic electrode, single-use Electrode conductive medium

QuickScan Pads & Electrodes Pack by Precision Biometrics Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Precision Biometrics Inc

Sources (1)

FDA UDI 126f20b8-699a-45ec-b9be-fe9b221027d1 33 fields · synced May 30, 2026