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TeleRehab Receiver Box

FDA UDI

Class II (US FDA UDI)

by Scottcare Corporation, The

Identity

Trade Name
TeleRehab Receiver Box FDA UDI
Generic Name
Electrocardiography monitoring system receiver FDA UDI
Device Name
The housing used to enclose RF receiver cards for use with the TeleRehab system. FDA UDI
Model / Reference
TR620 FDA UDI
Description
The housing used to enclose RF receiver cards for use with the TeleRehab system. FDA UDI

Identifiers

Catalog Number
101127 FDA UDI
Primary DI / UDI-DI
00856298006282 FDA UDI
510(k) Number
K050778 FDA UDI
FDA Product Code
DRG FDA UDI
GMDN Term
Electrocardiography monitoring system receiver FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.2910 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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Electrocardiography monitoring system receiver

TeleRehab Receiver Box by Scottcare Corporation, The — 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 8b1a9452-7548-4eba-9e95-d27a4ae8bc19 36 fields · synced May 30, 2026