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New Deantronics E0560SI

by New Deantronics Taiwan, Ltd.

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

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 Number20813527027429 UDI-DI Date30 Jun 2017ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
New Deantronics
Generic Name
Electrical-only medical device connection cable, reusable
Model / Reference
E0560SI
Primary DI / UDI-DI
20813527027429
FDA Product Code
GEI
GMDN Term
Electrical-only medical device connection cable, reusable
Device Class
Class II
Regulation Number
878.4400
GUDID distribution status
In Commercial Distribution

Other devices from New Deantronics Taiwan, Ltd.

See all devices from New Deantronics Taiwan, Ltd. →

Properties

  • Single Use
  • Prescription Use
  • Lot / Batch Number
  • Manufacturing Date

Other properties (10)

  • Sterile: 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