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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
5 Lead Patient Cable, IEC, HR300 FDA UDI
Model / Reference
001-400-0095 FDA UDI
Description
5 Lead Patient Cable, IEC, HR300 FDA UDI

Identifiers

Catalog Number
711059 FDA UDI
Primary DI / UDI-DI
90815187020122 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 06deff6e-6c7b-4b7d-9728-ac007a18bb30 35 fields · synced May 30, 2026