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Watchman®

FDA UDI

Class III (US FDA UDI)

by Boston Scientific

Identity

Trade Name
WATCHMAN® FDA UDI
Generic Name
Cardiac defect occluder FDA UDI
Device Name
Left Atrial Appendage Closure Device with Delivery System FDA UDI
Model / Reference
M635WU24060 FDA UDI
Description
Left Atrial Appendage Closure Device with Delivery System FDA UDI

Identifiers

Catalog Number
M635WU24060 FDA UDI
Primary DI / UDI-DI
08714729838234 FDA UDI
PMA Number
P130013 FDA UDI
FDA Product Code
NGV FDA UDI
GMDN Term
Cardiac defect occluder FDA UDI

Classification

Device Class
Class III FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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: Cardiac defect occluder

Watchman® by Boston Scientific — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Cardiac defect occluder.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Boston Scientific

Sources (1)

  • FDA UDI e4e0196a-c036-4586-8b9a-c7711dc3d3f5 36 fields · synced Jun 6, 2026