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Walrus A 416N-W

by CODAN US Corporation

Walrus A 416N-W is a Class II device made by CODAN US Corporation, listed in FDA GUDID since 20 Sep 2016 (UDI-DI 10813153020552), 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 Number10813153020552 UDI-DI Date20 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  • Withdrawn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
Walrus
Generic name
Basic intravenous administration set, noninvasive
Model / reference
A 416N-W
Primary DI / UDI-DI
10813153020552
FDA product code
FPA
GMDN term
Basic intravenous administration set, noninvasive
Device class
Class II
Regulation number
880.5440
GUDID distribution status
In Commercial Distribution

Related devices

Category: Basic intravenous administration set, noninvasive

Other devices from CODAN US Corporation

See all devices from CODAN US Corporation →

Properties

  • Supplied sterile
  • Single use
  • Lot / batch number
  • Expiration date
Other properties (11, all answered No)