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Coaxial needle COX-2000-18-0101

by Möller Medical GmbH

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 Number04260277175122 UDI-DI Date17 Aug 2018ListedStatusListed 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  • Withdrawn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
Coaxial needle
Generic Name
Needle guide, single-use
Model / Reference
COX-2000-18-0101
Primary DI / UDI-DI
04260277175122
FDA Product Code
KNW
GMDN Term
Needle guide, single-use
Device Class
Class II
Regulation Number
876.1075
GUDID distribution status
In Commercial Distribution

Related devices

Category: Needle guide, single-use

Other devices from Möller Medical GmbH

See all devices from Möller Medical GmbH →

Properties

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

Other properties (8)

  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No