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DORO® Reusable Bipolar Cable 5015-12

by Black Forest Medical GmbH

Listed FDA GUDID listing, not in commercial distribution

Valid until

Not applicable

Database listing, no authorization

FDA recalls

None found

in data synced 23 Oct 2026

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number04250435504963 UDI-DI Date8 Dec 2016ListedStatusListed GUDID: not in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 23 Oct 2026.

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name
DORO® Reusable Bipolar Cable
Generic Name
Electrical-only medical device connection cable, reusable
Model / Reference
5015-12
Primary DI / UDI-DI
04250435504963
510(k) Number
FDA Product Code
GEI
GMDN Term
Electrical-only medical device connection cable, reusable
Device Class
Class II
Regulation Number
878.4400
GUDID distribution status
Not in Commercial Distribution

Related devices

Cleared under the same submission (K070997)

Other devices from Black Forest Medical GmbH

See all devices from Black Forest Medical GmbH →

Properties

  • Prescription Use
  • Lot / Batch Number

Other properties (12)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Expiration Date: No
  • Manufacturing Date: No