← Back to catalogue

Bloom2

FDA UDI

Class II (US FDA UDI)

by Fischer Medical

Identity

Trade Name
Bloom2 FDA UDI
Generic Name
Cardiac electrophysiology stimulation system FDA UDI
Device Name
Bloom2 Cardiac Stimulator System: External Programmable Pacemaker Pulse Generator FDA UDI
Model / Reference
Bloom2 Console FDA UDI
Description
Bloom2 Cardiac Stimulator System: External Programmable Pacemaker Pulse Generator FDA UDI

Identifiers

Catalog Number
370050G FDA UDI
Primary DI / UDI-DI
00863019000351 FDA UDI
510(k) Number
K173439 FDA UDI
FDA Product Code
JOQ FDA UDI
GMDN Term
Cardiac electrophysiology stimulation system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1750 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Cardiac electrophysiology stimulation system

Bloom2 by Fischer Medical — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Cardiac electrophysiology stimulation system.

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
Fischer Medical

Sources (1)

  • FDA UDI b78e066c-fada-450f-b013-8d5094f71eee 35 fields · synced May 30, 2026