Skip to content

CORFLO cuBBy LPGD 35-2415

by Corpak Medsystems

CORFLO cuBBy LPGD 35-2415 is a Class II device made by Corpak Medsystems, listed in FDA GUDID since 4 Aug 2016 (UDI-DI 10815149025190), 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 Number10815149025190 UDI-DI Date4 Aug 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  • Withdrawn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
CORFLO cuBBy LPGD
Generic name
Gastrostomy button
Model / Ref / Catalog
35-2415
Primary DI / UDI-DI
10815149025190
FDA product code
KNT
GMDN term
Gastrostomy button
Device class
Class II
Regulation number
876.5980
GUDID distribution status
In Commercial Distribution
Sterilisation method
Ethylene Oxide
Size
Catheter Gauge — 24 French
Length — 1.5 Centimeter

Related devices

Category: Gastrostomy button

Other devices from Corpak Medsystems

See all devices from Corpak Medsystems →

Properties

  • Supplied sterile
  • Sterilise before use
  • Single use
  • Implantable
  • Prescription use
  • Convenience kit
  • Lot / batch number
  • Expiration date
Other properties (7, all answered No)