← Back to catalogue

AtriClip® LAA Exclusion System

FDA UDI

Class I (US FDA UDI)

by Atricure, Inc.

Identity

Trade Name
AtriClip® LAA Exclusion System FDA UDI
Generic Name
Surgical implant template, single-use FDA UDI
Device Name
Selection Guide, AOD1 FDA UDI
Model / Reference
CGG FDA UDI
Description
Selection Guide, AOD1 FDA UDI

Identifiers

Catalog Number
A000349 FDA UDI
Primary DI / UDI-DI
00818354010497 FDA UDI
FDA Product Code
FZX FDA UDI
GMDN Term
Surgical implant template, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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

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

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Conditional FDA UDI

Category: Surgical implant template, single-use

AtriClip® LAA Exclusion System by Atricure, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical implant template, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Atricure, Inc.

Sources (1)

  • FDA UDI 94c86b10-e37e-4699-95d3-d380262a36c5 35 fields · synced May 30, 2026