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EZLink

FDA UDI

Class II (US FDA UDI)

by Scottcare Corporation, The

Identity

Trade Name
EZLink FDA UDI
Generic Name
Cardiology information system application software FDA UDI
Model / Reference
EZLink FDA UDI

Identifiers

Catalog Number
100076 FDA UDI
Primary DI / UDI-DI
00856298006183 FDA UDI
510(k) Number
K020213 FDA UDI
FDA Product Code
DXH FDA UDI
GMDN Term
Cardiology information system application software FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.2920 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Cardiology information system application software

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

Similar devices

Also classified as Cardiology information system application software.

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 33b04d2e-d5ef-48bd-896b-5b3703ce3bb8 35 fields · synced Jun 8, 2026