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SmartClaw™ FD0660-02

by Boston Scientific

SmartClaw™ FD0660-02 is a Class II device made by Boston Scientific, listed in FDA GUDID since 5 Jun 2024 (UDI-DI 00191506050023), registry data as of 23 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00191506050023 UDI-DI Date5 Jun 2024ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
SmartClaw™
Generic name
Thrombectomy suction catheter
Model / Ref / Catalog
FD0660-02
Primary DI / UDI-DI
00191506050023
FDA product code
QEW
GMDN term
Thrombectomy suction catheter
Device class
Class II
Regulation number
870.5150
GUDID distribution status
In Commercial Distribution
Size
Outer Diameter — 32 Millimeter

Related devices

Category: Thrombectomy suction catheter

Similar devices in this category

Other devices filed under Thrombectomy suction catheter.

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Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Lot / batch number
  • Expiration date
Other properties (10, all answered No)