Skip to content

Performa® 00884450362044

by Merit Medical Systems, Inc.

Performa® 00884450362044 (PV512538MP2SH/A) is a Class II device made by Merit Medical Systems, Inc., listed in FDA GUDID since 6 Apr 2018 (UDI-DI 00884450362044), 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 Number00884450362044 UDI-DI Date6 Apr 2018ListedStatusListed 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  • Withdrawn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
Performa®
Generic name
Angiographic catheter, single-use
Model / Ref / Catalog
00884450362044, PV512538MP2SH/A
Primary DI / UDI-DI
00884450362044
FDA product code
DQO
GMDN term
Angiographic catheter, single-use
Device class
Class II
Regulation number
870.1200
GUDID distribution status
In Commercial Distribution

Related devices

Category: Angiographic catheter, single-use

Similar devices in this category

Other devices filed under Angiographic catheter, single-use.

Other devices from Merit Medical Systems, Inc.

See all devices from Merit Medical Systems, Inc. →

Properties

  • Supplied sterile
  • Single use
  • Lot / batch number
  • Expiration date
Other properties (11, all answered No)