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Xhibit

FDA UDI

Class II (US FDA UDI)

by Spacelabs Healthcare (washington), Inc

Identity

Trade Name
Xhibit FDA UDI
Generic Name
Electrocardiography monitoring system receiver FDA UDI
Device Name
KIT, DOWN CONVERTER, ACTIVE ANTENNA FDA UDI
Model / Reference
Xhibit Central FDA UDI
Description
KIT, DOWN CONVERTER, ACTIVE ANTENNA FDA UDI

Identifiers

Catalog Number
040-1486-01 FDA UDI
Primary DI / UDI-DI
10841522102882 FDA UDI
510(k) Number
K141156 FDA UDI
FDA Product Code
DSI FDA UDI
GMDN Term
Electrocardiography monitoring system receiver 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

Yes

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

Yes

FDA UDI

Category: Electrocardiography monitoring system receiver

Xhibit by Spacelabs Healthcare (washington), Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electrocardiography monitoring system receiver.

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 e6a6eb28-8d43-4d02-aea4-f6ea76d5c187 36 fields · synced Jun 1, 2026