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WiSE CRT System

FDA UDI

Class III (US FDA UDI)

by EBR Systems, Inc.

Identity

Trade Name
WiSE CRT System FDA UDI
Generic Name
Cardiac pulse generator programmer FDA UDI
Device Name
Programmer FDA UDI
Model / Reference
5100 FDA UDI
Description
Programmer FDA UDI

Identifiers

Primary DI / UDI-DI
00859244007296 FDA UDI
PMA Number
P240028 FDA UDI
FDA Product Code
SEG FDA UDI
GMDN Term
Cardiac pulse generator programmer FDA UDI

Classification

Device Class
Class III 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

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Cardiac pulse generator programmer

WiSE CRT System by EBR Systems, Inc. — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Cardiac pulse generator programmer.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
EBR Systems, Inc.

Sources (1)

  • FDA UDI 6368a569-afcb-4fac-86fb-375fbc24af60 36 fields · synced Jun 8, 2026