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Glooko Web Application

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref REF-0001

by Glooko, Inc.

Identity

Trade Name
Glooko Web Application EUDAMEDFDA UDI
Generic Name
Clinical management support software FDA UDI
Device Name
Glooko Web Application EUDAMED
Glooko Web Application is a web based application that displays and analyzes retrospective data that is captured from BG meters, insulin pumps and continuous glucose monitors (CGM) FDA UDI
Model / Reference
REF-0001 EUDAMED
xx.yy (xx is model year and yy is a serial number) FDA UDI
Description
Glooko Web Application is a web based application that displays and analyzes retrospective data that is captured from BG meters, insulin pumps and continuous glucose monitors (CGM) FDA UDI

Identifiers

Primary DI / UDI-DI
00855093008026 EUDAMEDFDA UDI
Basic UDI-DI
0085509300WebAppRef001LF EUDAMED
FDA Product Code
PHV FDA UDI
EMDN Code
V92 MEDICAL DEVICE SOFTWARE - NOT INCLUDED IN OTHER CLASSES EUDAMED
GMDN Term
Clinical management support software FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class I FDA UDI
Regulation Number
862.2120 FDA UDI
Special Device Type
Software EUDAMED
Market of Registration
Sweden EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Prescription Use

No

FDA UDI

Over-the-Counter

Yes

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Glooko Web Application by Glooko, Inc. — Class IIa — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Glooko, Inc.
EUDAMED SRN
US-MF-000023483
Authorised Representative
MedEnvoy Global BV NL-AR-000024028

Sources (2)

  • EUDAMED 724a058e-d721-45af-9007-74d1807c9213 61 fields · synced Jun 18, 2026
  • FDA UDI 67928ef8-980b-4035-866a-eac9fa4cc3f1 33 fields · synced May 30, 2026