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Xhibit Telemetry Receiver

FDA UDI

Class II (US FDA UDI)

by Spacelabs Healthcare (washington), Inc

Identity

Trade Name
Xhibit Telemetry Receiver FDA UDI
Generic Name
Electrocardiography monitoring system receiver FDA UDI
Device Name
ANTENNA,UHF,450-470MHZ, ROHS, UDI FDA UDI
Model / Reference
Xhibit Telemetry Receiver FDA UDI
Description
ANTENNA,UHF,450-470MHZ, ROHS, UDI FDA UDI

Identifiers

Catalog Number
011-0247-01 FDA UDI
Primary DI / UDI-DI
10841522120190 FDA UDI
510(k) Number
K141156 FDA UDI
FDA Product Code
MLD FDA UDI
MSX FDA UDI
MHX FDA UDI
DSI FDA UDI
GMDN Term
Electrocardiography monitoring system receiver FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1025 FDA UDI
870.2300 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

Yes

FDA UDI

Category: Electrocardiography monitoring system receiver

Xhibit Telemetry Receiver 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 5efedd0b-9ce7-4351-a440-f7e58ef6859c 35 fields · synced May 30, 2026