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eNcounter

FDA UDI

Class I (US FDA UDI)

by GlobalMed Holdings, LLC

Identity

Trade Name
eNcounter FDA UDI
Generic Name
Patient health record information system FDA UDI
Device Name
A complete telehealth platform that offers secure telemedicine software solutions with diagnostic and clinical workflow capabilities combined with interoperable services that work with an existing platform including scheduling, video consultations, data integration, and integration management services. FDA UDI
Model / Reference
eNcounter FDA UDI
Description
A complete telehealth platform that offers secure telemedicine software solutions with diagnostic and clinical workflow capabilities combined with interoperable services that work with an existing platform including scheduling, video consultations, data integration, and integration management services. FDA UDI

Identifiers

Primary DI / UDI-DI
00850033167115 FDA UDI
FDA Product Code
OUG FDA UDI
GMDN Term
Patient health record information system FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6310 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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Patient health record information system

eNcounter by GlobalMed Holdings, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Patient health record information system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 9759d3a9-e092-481a-9878-2afd3c9e9d24 33 fields · synced Jun 9, 2026