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FlowSaver AS-01189/ 80-101

by Inari Medical, Inc.

FlowSaver AS-01189/ 80-101 is a Class II device made by Inari Medical, Inc., listed in FDA GUDID since 29 May 2024 (UDI-DI 00810123710546), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00810123710546 UDI-DI Date29 May 2024ListedStatusListed 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  • Withdrawn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
FlowSaver
Generic name
Blood transfusion filter
Model / Ref / Catalog
AS-01189/ 80-101, 80-101
Primary DI / UDI-DI
00810123710546
FDA product code
CAC
GMDN term
Blood transfusion filter
Device class
Class II
Regulation number
868.5830
GUDID distribution status
In Commercial Distribution

Related devices

Category: Blood transfusion filter

Similar devices in this category

Other devices filed under Blood transfusion filter.

Other devices from Inari Medical, Inc.

See all devices from Inari Medical, Inc. →

Properties

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