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Protekt VX 5000 PMVSM5000

by Proactive Medical Products

Protekt VX 5000 PMVSM5000 is a Class II device made by Proactive Medical Products, listed in FDA GUDID since 18 Dec 2025 (UDI-DI 05061105057455), 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 Number05061105057455 UDI-DI Date18 Dec 2025ListedStatusListed 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  • Withdrawn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
Protekt VX 5000
Generic name
MRI-patient physiologic monitoring system
Model / Ref / Catalog
PMVSM5000
Primary DI / UDI-DI
05061105057455
FDA product code
FNM
GMDN term
MRI-patient physiologic monitoring system
Device class
Class II
Regulation number
880.5550
GUDID distribution status
In Commercial Distribution
Size
Height — 40 Inch
Width — 18 Inch
Length — 16 Inch

Similar devices

Other devices filed under FDA product code FNM (Mattress, Air Flotation, Alternating Pressure).

Other devices from Proactive Medical Products

See all devices from Proactive Medical Products →

Properties

  • Convenience kit
  • Premarket exempt
  • Lot / batch number
  • Serial number
  • Manufacturing date
Other properties (10, all answered No)