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Emerge™ H7493918920250

by Boston Scientific

Emerge™ H7493918920250 is a Class II device made by Boston Scientific, listed in FDA GUDID since 24 Sep 2016 (UDI-DI 08714729806325), 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 Number08714729806325 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  • Withdrawn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
Emerge™
Generic name
Coronary angioplasty balloon catheter, basic
Model / reference
H7493918920250
Primary DI / UDI-DI
08714729806325
FDA product code
LOX
GMDN term
Coronary angioplasty balloon catheter, basic
Device class
Class II
Regulation number
870.5100
GUDID distribution status
In Commercial Distribution

Related devices

Category: Coronary angioplasty balloon catheter, basic

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)