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FLO30™ 00884450036570

by Merit Medical Systems, Inc.

FLO30™ 00884450036570 is a Class II device made by Merit Medical Systems, Inc., listed in FDA GUDID since 10 Oct 2016 (UDI-DI 00884450036570), 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 Number00884450036570 UDI-DI Date10 Oct 2016ListedStatusListed 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  • Withdrawn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
FLO30™
Generic name
Haemostasis valve
Model / reference
00884450036570
Primary DI / UDI-DI
00884450036570
FDA product code
DTL
GMDN term
Haemostasis valve
Device class
Class II
Regulation number
870.4290
GUDID distribution status
In Commercial Distribution

Related devices

Category: Angiography kitHaemostasis valve

Similar devices in this category

Other devices filed under Haemostasis valve.

Other devices from Merit Medical Systems, Inc.

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Properties

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