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RunWay™ H749389697430

by Boston Scientific

RunWay™ H749389697430 is a Class II device made by Boston Scientific, listed in FDA GUDID since 1 Feb 2018 (UDI-DI 08714729965183), 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 Number08714729965183 UDI-DI Date1 Feb 2018ListedStatusListed 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  • Withdrawn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
RunWay™
Generic name
Vascular guide-catheter, single-use
Model / reference
H749389697430
Primary DI / UDI-DI
08714729965183
FDA product code
DQY
GMDN term
Vascular guide-catheter, single-use
Device class
Class II
Regulation number
870.1250
GUDID distribution status
In Commercial Distribution

Related devices

Category: Vascular guide-catheter, single-use

Similar devices in this category

Other devices filed under Vascular guide-catheter, single-use.

Other devices from Boston Scientific

See all devices from Boston Scientific →

Properties

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