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Labsystem™ Pro

FDA UDI

Class II (US FDA UDI)

by Boston Scientific

Identity

Trade Name
LABSYSTEM™ PRO FDA UDI
Generic Name
Multiple physiological signal amplifier FDA UDI
Device Name
CLEARSIGN™ II Amplifier For LABSYSTEM™ PRO EP Recording System, 40 Channels FDA UDI
Model / Reference
M00420020210 FDA UDI
Description
CLEARSIGN™ II Amplifier For LABSYSTEM™ PRO EP Recording System, 40 Channels FDA UDI

Identifiers

Catalog Number
M00420020210 FDA UDI
Primary DI / UDI-DI
08714729884842 FDA UDI
FDA Product Code
DRQ FDA UDI
GMDN Term
Multiple physiological signal amplifier FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.2060 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: Multiple physiological signal amplifier

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

Similar devices

Also classified as Multiple physiological signal amplifier.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Boston Scientific

Sources (1)

  • FDA UDI bc803e69-4057-4a19-87a5-709116586b7e 34 fields · synced May 30, 2026