Skip to content

Ellipse™ CD1411-36Q

by St. Jude Medical, Inc.

Ellipse™ CD1411-36Q is a Class III device made by St. Jude Medical, Inc., listed in FDA GUDID since 2 Feb 2017 (UDI-DI 05414734507738), 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 Number05414734507738 UDI-DI Date2 Feb 2017ListedStatusListed 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  • Withdrawn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
Ellipse™
Generic name
Single-chamber implantable defibrillator
Model / Ref / Catalog
CD1411-36Q
Primary DI / UDI-DI
05414734507738
FDA product code
NVZ
GMDN term
Single-chamber implantable defibrillator
Device class
Class III
GUDID distribution status
In Commercial Distribution
MRI safety
MR Conditional
Size
Total Volume — 30.2 Milliliter

Related devices

Category: Single-chamber implantable defibrillator

Similar devices

Other devices filed under FDA product code NVZ (Pulse generator, permanent, implantable).

Other devices from St. Jude Medical, Inc.

See all devices from St. Jude Medical, Inc. →

Properties

  • Supplied sterile
  • Single use
  • Implantable
  • Prescription use
  • Serial number
  • Expiration date
Other properties (9, all answered No)