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Patient Cable

FDA UDI

Class II (US FDA UDI)

by Global Instrumentation, Llc

Identity

Trade Name
Patient Cable FDA UDI
Generic Name
Electrocardiographic ambulatory recorder FDA UDI
Device Name
7 Lead Patient Cable, AHA, HR100 FDA UDI
Model / Reference
004-400-0006 FDA UDI
Description
7 Lead Patient Cable, AHA, HR100 FDA UDI

Identifiers

Catalog Number
704547 FDA UDI
Primary DI / UDI-DI
90815187020221 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

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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Electrocardiographic ambulatory recorder

Patient Cable 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

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Manufacturer

Sources (1)

  • FDA UDI 572d73a7-0f7a-4ee3-80e1-5052c19a9931 35 fields · synced May 30, 2026