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BioFlo 46710

by Navilyst Medical, Inc.

BioFlo 46710 is a Class II device made by Navilyst Medical, Inc., listed in FDA GUDID since 20 Sep 2016 (UDI-DI H965467100), 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 NumberH965467100 UDI-DI Date20 Sep 2016ListedStatusListed 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  • Withdrawn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
BioFlo
Generic name
Peripheral intravenous cannula
Model / reference
46710
Primary DI / UDI-DI
H965467100
FDA product code
FOZ
GMDN term
Peripheral intravenous cannula
Device class
Class II
Regulation number
880.5200
GUDID distribution status
In Commercial Distribution
Size
Catheter Gauge — 5 French
Needle Gauge — 21 Gauge
Length — 20 Centimeter
Outer Diameter — 1.68 Millimeter

Related devices

Category: Peripheral intravenous cannula

Similar devices in this category

Other devices filed under Peripheral intravenous cannula.

Other devices from Navilyst Medical, Inc.

See all devices from Navilyst Medical, Inc. →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Lot / batch number
  • Expiration date
Other properties (10, all answered No)