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VistaPhone

FDA UDI

Class II (US FDA UDI)

by VitalConnect, Inc.

Identity

Trade Name
VistaPhone FDA UDI
Generic Name
Multiple vital physiological parameter monitoring system transceiver FDA UDI
Device Name
Vista Phone S9 relay device FDA UDI
Model / Reference
8303-03 FDA UDI
Description
Vista Phone S9 relay device FDA UDI

Identifiers

Catalog Number
8303-03 FDA UDI
Primary DI / UDI-DI
00850490007481 FDA UDI
510(k) Number
K193343 FDA UDI
FDA Product Code
DRG FDA UDI
GMDN Term
Multiple vital physiological parameter monitoring system transceiver 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

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Multiple vital physiological parameter monitoring system transceiver

VistaPhone by VitalConnect, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
VitalConnect, Inc.

Sources (1)

  • FDA UDI 061e70e3-6fa5-4838-b283-d8f50055baf2 35 fields · synced Jun 8, 2026