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FlowSaver

FDA UDI

Class II (US FDA UDI)

by Inari Medical, Inc.

Identity

Trade Name
FlowSaver FDA UDI
Generic Name
Blood transfusion filter FDA UDI
Device Name
FlowSaver FDA UDI
Model / Reference
AS-01189/ 80-101 FDA UDI
Description
FlowSaver FDA UDI

Identifiers

Catalog Number
80-101 FDA UDI
Primary DI / UDI-DI
00810123710546 FDA UDI
FDA Product Code
CAC FDA UDI
GMDN Term
Blood transfusion filter FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5830 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Blood transfusion filter

FlowSaver by Inari Medical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Blood transfusion filter.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Inari Medical, Inc.

Sources (1)

  • FDA UDI 7877ebaa-92b7-436f-bb6e-1d2707d3afb4 35 fields · synced May 29, 2026