Endotak Reliance® Sg

FDA UDI

Class III (US FDA UDI)

by Boston Scientific

Identity

Trade Name: ENDOTAK RELIANCE® SG FDA UDI
Generic Name: Endocardial defibrillation lead FDA UDI
Device Name: Steroid-eluting Bipolar Pace/Sense and Defibrillation Lead FDA UDI
Model / Reference: 0293 FDA UDI
Description: Steroid-eluting Bipolar Pace/Sense and Defibrillation Lead FDA UDI

Identifiers

Primary DI / UDI-DI: 00802526531255 FDA UDI
PMA Number: P910073 FDA UDI
FDA Product Code: NVY FDA UDI
GMDN Term: Endocardial defibrillation lead FDA UDI

Classification

Device Class: Class III FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

Yes

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

MRI Safety

MR Conditional FDA UDI

Category: Endocardial defibrillation lead

Endotak Reliance® Sg by Boston Scientific — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Cleared under the same submission

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 III	Pending data

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Manufacturer

Manufacturer: Boston Scientific

Sources (1)

FDA UDI 189c630b-9583-4fa6-add0-447a56929efe 35 fields · synced May 30, 2026