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AngioDynamics 91425

by Navilyst Medical, Inc.

AngioDynamics 91425 is a device made by Navilyst Medical, Inc., listed in FDA GUDID since 13 Aug 2018 (UDI-DI H965914250), 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 NumberH965914250 UDI-DI Date13 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  • Withdrawn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
AngioDynamics
Generic name
Catheter/overtube balloon inflator, single-use
Model / reference
91425
Primary DI / UDI-DI
H965914250
GMDN term
Catheter/overtube balloon inflator, single-use
GUDID distribution status
In Commercial Distribution
Size
Pressure — 3040 KiloPascal

Related devices

Category: Catheter/overtube balloon inflator, single-use

Similar devices in this category

Other devices filed under Catheter/overtube balloon inflator, single-use.

Other devices from Navilyst Medical, Inc.

See all devices from Navilyst Medical, Inc. →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Convenience kit
  • Lot / batch number
  • Expiration date
Other properties (9, all answered No)