Skip to content

FORCECORD Passing Probe MPDP3020

by Xiros Ltd

FORCECORD Passing Probe MPDP3020 is a Class I device made by Xiros Ltd, listed in FDA GUDID since 6 Jul 2026 (UDI-DI 05060267134554), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number05060267134554 UDI-DI Date6 Jul 2026ListedStatusListed 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  • Withdrawn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
FORCECORD Passing Probe
Generic name
Exploratory blunt needle, single-use
Model / reference
MPDP3020
Primary DI / UDI-DI
05060267134554
FDA product code
HXB
GMDN term
Exploratory blunt needle, single-use
Device class
Class I
Regulation number
888.4540
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code HXB (Probe).

Other devices from Xiros Ltd

See all devices from Xiros Ltd →

Properties

  • Supplied sterile
  • Single use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (10, all answered No)