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Woven M0046FMC007490

by Boston Scientific

Woven M0046FMC007490 is a Class II device made by Boston Scientific, listed in FDA GUDID since 24 Sep 2016 (UDI-DI 08714729901693), 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 Number08714729901693 UDI-DI Date24 Sep 2016ListedStatusListed 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  • Withdrawn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
Woven
Generic name
Cardiac mapping catheter, percutaneous, single-use
Model / reference
M0046FMC007490
Primary DI / UDI-DI
08714729901693
FDA product code
DRF
GMDN term
Cardiac mapping catheter, percutaneous, single-use
Device class
Class II
Regulation number
870.1220
GUDID distribution status
In Commercial Distribution

Related devices

Category: Cardiac mapping catheter, percutaneous, single-use

Similar devices in this category

Other devices filed under Cardiac mapping catheter, percutaneous, single-use.

Other devices from Boston Scientific

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Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (9, all answered No)