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iLab™

FDA UDI

Class II (US FDA UDI)

by Boston Scientific

Identity

Trade Name
iLab™ FDA UDI
Generic Name
Cardiovascular ultrasound imaging system FDA UDI
Device Name
Cart Refurb System FDA UDI
Model / Reference
M004EPIL120CARTR0 FDA UDI
Description
Cart Refurb System FDA UDI

Identifiers

Primary DI / UDI-DI
08714729810087 FDA UDI
FDA Product Code
DQK FDA UDI
GMDN Term
Cardiovascular ultrasound imaging system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1425 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

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Cardiovascular ultrasound imaging system

iLab™ by Boston Scientific — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Cardiovascular ultrasound imaging system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Boston Scientific

Sources (1)

  • FDA UDI f451ceb0-db3b-4abe-8111-8bb87ab4a43d 33 fields · synced Jun 1, 2026