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Ablacath System Interconnect Cable AB-0005

by Ablacon Inc.

Ablacath System Interconnect Cable AB-0005 is a Class II device made by Ablacon Inc., listed in FDA GUDID since 21 Feb 2025 (UDI-DI 00860457001520), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00860457001520 UDI-DI Date21 Feb 2025ListedStatusListed 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  • Withdrawn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
Ablacath System Interconnect Cable
Generic name
Electrical-only medical device connection cable, reusable
Model / reference
AB-0005
Primary DI / UDI-DI
00860457001520
FDA product code
IKD
GMDN term
Electrical-only medical device connection cable, reusable
Device class
Class II
Regulation number
890.1175
GUDID distribution status
In Commercial Distribution

Related devices

Category: Electrical-only medical device connection cable, reusable

Similar devices in this category

Other devices filed under Electrical-only medical device connection cable, reusable.

Other devices from Ablacon Inc.

See all devices from Ablacon Inc. →

Properties

  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (11, all answered No)