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Neptune 0700007000

by Stryker Corp.

Listed FDA GUDID listing, not in commercial distribution

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 Number04546540916389 UDI-DI Date17 Oct 2016ListedStatusListed GUDID: not 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  • Withdrawn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
Neptune
Generic name
Surgical fluid/smoke waste management system
Model / Ref / Catalog
0700007000, 0700-007-000
Primary DI / UDI-DI
04546540916389
FDA product code
GCX
GMDN term
Surgical fluid/smoke waste management system
Device class
Class II
Regulation number
880.6740
GUDID distribution status
Not in Commercial Distribution

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Properties

  • Prescription use
  • Premarket exempt
  • Serial number

Other properties (12)

  • Supplied sterile: No
  • Sterilise before use: No
  • Single use: No
  • Implantable: No
  • Contains latex: No
  • Over-the-counter: No
  • Convenience kit: No
  • Combination product: No
  • HCT/P: No
  • Lot / batch number: No
  • Expiration date: No
  • Manufacturing date: No