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FlowStasis Single-Pack

FDA UDIEUDAMED

Class I (US FDA UDI)

by Inari Medical, Inc.

Identity

Trade Name
FlowStasis Single-Pack FDA UDI
Generic Name
Suture retention device FDA UDI
Device Name
FlowStasis Single-Pack FDA UDI
Model / Reference
70-103 FDA UDI
Description
FlowStasis Single-Pack FDA UDI

Identifiers

Catalog Number
70-103 FDA UDI
Primary DI / UDI-DI
00850291007420 FDA UDI
FDA Product Code
KGS FDA UDI
GMDN Term
Suture retention device FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4930 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Suture retention device

FlowStasis Single-Pack by Inari Medical, Inc. — Class I — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Suture retention device.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDR

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Inari Medical, Inc.

Sources (2)

  • FDA UDI 967d0aeb-9628-40b3-9e17-4cf756498f70 35 fields · synced Jun 18, 2026
  • EUDAMED 1 fields · synced Jun 18, 2026