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AtriCure System Cart

FDA UDI

Class I (US FDA UDI)

by Atricure, Inc.

Identity

Trade Name
AtriCure System Cart FDA UDI
Generic Name
Instrument trolley FDA UDI
Device Name
Basic Cart FDA UDI
Model / Reference
ASCB2 FDA UDI
Description
Basic Cart FDA UDI

Identifiers

Catalog Number
A000842 FDA UDI
Primary DI / UDI-DI
10840143901522 FDA UDI
FDA Product Code
HMF FDA UDI
GMDN Term
Instrument trolley FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
886.1860 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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Instrument trolley

AtriCure System Cart by Atricure, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Instrument trolley.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Atricure, Inc.

Sources (1)

  • FDA UDI 8bdb88da-072a-4292-a27f-70e3e80becd8 36 fields · synced Jun 8, 2026