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Echotip Insight

FDA UDI

Class II (US FDA UDI)

by Cook Ireland, Ltd.

Identity

Trade Name
Echotip Insight FDA UDI
Generic Name
Endoscopic portal pressure measurement system FDA UDI
Device Name
Echotip Insight Portosystemic Pressure Gradient Measurement System FDA UDI
Model / Reference
G46560 FDA UDI
Description
Echotip Insight Portosystemic Pressure Gradient Measurement System FDA UDI

Identifiers

Catalog Number
ECHO-PPG FDA UDI
Primary DI / UDI-DI
00827002465602 FDA UDI
FDA Product Code
QIJ FDA UDI
GMDN Term
Endoscopic portal pressure measurement system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1050 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Endoscopic portal pressure measurement system

Echotip Insight by Cook Ireland, Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cook Ireland, Ltd.

Sources (1)

  • FDA UDI 20d69606-a004-4c63-a651-ce8856aa1902 36 fields · synced Jun 6, 2026