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Cannula Standard Without Stylet

by Alpha Omega Engineering Corp.

Cannula Standard Without Stylet (366-015521-00) is a Class II device made by Alpha Omega Engineering Corp., listed in FDA GUDID since 24 Sep 2016 (UDI-DI 07290016450729), 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 Number07290016450729 UDI-DI Date24 Sep 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  • Withdrawn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
Cannula
Generic name
Intracerebral cannula, implantable
Model / Ref / Catalog
Standard Without Stylet, 366-015521-00
Primary DI / UDI-DI
07290016450729
FDA product code
GZL
GMDN term
Intracerebral cannula, implantable
Device class
Class II
Regulation number
882.1330
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization
MRI safety
MR Unsafe

Similar devices

Other devices filed under FDA product code GZL (Electrode, Depth).

Other devices from Alpha Omega Engineering Corp.

See all devices from Alpha Omega Engineering Corp. →

Properties

  • Sterilise before use
  • Single use
  • Implantable
  • Prescription use
  • Lot / batch number
  • Expiration date
Other properties (9, all answered No)