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PER900 Preventice

FDA UDI

Class II (US FDA UDI)

by Braemar Manufacturing, LLC

Identity

Trade Name
PER900 Preventice FDA UDI
Generic Name
Electrocardiography telemetric monitoring system FDA UDI
Device Name
ENHANCED ALGORITHM ECG EVENT RECORDER FDA UDI
Model / Reference
900-0553-06 FDA UDI
Description
ENHANCED ALGORITHM ECG EVENT RECORDER FDA UDI

Identifiers

Primary DI / UDI-DI
B146PERP0 FDA UDI
510(k) Number
K071011 FDA UDI
FDA Product Code
MWJ FDA UDI
GMDN Term
Electrocardiography telemetric monitoring system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.2800 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Electrocardiography telemetric monitoring system

PER900 Preventice by Braemar Manufacturing, LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electrocardiography telemetric monitoring system.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI da74d3b4-11e8-498c-a9c6-985d10cf3a64 34 fields · synced Jun 9, 2026