TeleRehab Rack Server

FDA UDI

Class II (US FDA UDI)

by Scottcare Corporation, The

Identity

Trade Name: TeleRehab Rack Server FDA UDI
Generic Name: Network server FDA UDI
Model / Reference: TeleRehab Rack Server FDA UDI

Identifiers

Catalog Number: 100666 FDA UDI
Primary DI / UDI-DI: 00856298006305 FDA UDI
510(k) Number: K050778 FDA UDI
FDA Product Code: DRG FDA UDI
GMDN Term: Network server 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

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: Network server

TeleRehab Rack Server by Scottcare Corporation, The — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Network server.

TEK-CARE APPLIANCE SERVER, PAGE, 1 EV MON — Securitas Healthcare LLC · Class II
UbiqVue — LifeSignals, Inc. · Class II
UbiqVue — LifeSignals, Inc. · Class II
TEK-CARE LINUX SERVER, DESK-MOUNT — Securitas Healthcare LLC · Class II
ThinPrep Imaging System — Hologic, Inc. · Class III
3M™Filtek™ — 3M COMPANY · Class II
3M™Filtek™ — 3M COMPANY · Class II
3M™Filtek™ — 3M COMPANY · Class II

Cleared under the same submission

K050778 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer: Scottcare Corporation, The

Sources (1)

FDA UDI a7a06e30-6cd0-418a-b4e0-249de40c66fb 36 fields · synced Jun 1, 2026