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Bracket

FDA UDI

Class II (US FDA UDI)

by Global Instrumentation, Llc

Identity

Trade Name
Bracket FDA UDI
Generic Name
Electrocardiographic monitor FDA UDI
Device Name
ECG Mounting Accessory, ACM, WALL FDA UDI
Model / Reference
007-200-0136 FDA UDI
Description
ECG Mounting Accessory, ACM, WALL FDA UDI

Identifiers

Catalog Number
106550 FDA UDI
Primary DI / UDI-DI
90815187020030 FDA UDI
FDA Product Code
DSI FDA UDI
GMDN Term
Electrocardiographic monitor 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

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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Electrocardiographic monitor

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

Similar devices

Also classified as Electrocardiographic monitor.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 11006967-1550-4311-9167-74209a3e3a10 34 fields · synced May 30, 2026