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Refurbished 19-B Ir Remote Receiver

FDA UDI

Class II (US FDA UDI)

by Parks Medical Electronics, Inc.

Identity

Trade Name
REFURBISHED 19-B IR REMOTE RECEIVER FDA UDI
Generic Name
Cardiac arrhythmia monitoring system FDA UDI
Model / Reference
301-0376-00 FDA UDI

Identifiers

Primary DI / UDI-DI
00816787024289 FDA UDI
510(k) Number
K944495 FDA UDI
FDA Product Code
MHX FDA UDI
GMDN Term
Cardiac arrhythmia monitoring system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1025 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

Yes

FDA UDI

Category: Cardiac arrhythmia monitoring system

Refurbished 19-B Ir Remote Receiver by Parks Medical Electronics, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Cardiac arrhythmia 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 635c5184-21b3-4620-b3a0-062758a0c25d 34 fields · synced May 30, 2026