← Back to catalogue

Matrix Holter System

FDA UDI

Class II (US FDA UDI)

by Global Instrumentation, Llc

Identity

Trade Name
Matrix Holter System FDA UDI
Generic Name
Electrocardiographic ambulatory recorder FDA UDI
Device Name
M12R L Recorder, 10-Lead Cable, AHA, System Kit 90815187020184; M12R, 10 Lead patient Cable (DIN) 90815187020252; M12R Holter Recorder 90815187020320; M12R Carrying Case FDA UDI
Model / Reference
001-400-0123 FDA UDI
Description
M12R L Recorder, 10-Lead Cable, AHA, System Kit 90815187020184; M12R, 10 Lead patient Cable (DIN) 90815187020252; M12R Holter Recorder 90815187020320; M12R Carrying Case FDA UDI

Identifiers

Catalog Number
001-400-0123 FDA UDI
Primary DI / UDI-DI
90815187020719 FDA UDI
510(k) Number
K051730 FDA UDI
FDA Product Code
MLO FDA UDI
GMDN Term
Electrocardiographic ambulatory recorder 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

Yes

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

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: Electrocardiographic ambulatory recorder

Matrix Holter System by Global Instrumentation, Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electrocardiographic ambulatory recorder.

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

Sources (1)

  • FDA UDI f5c910ca-63ba-4a83-bdb3-7f2e0047ff8f 35 fields · synced Jun 8, 2026