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Rocket R54701

by Rocket Medical Plc

Rocket R54701 is a Class I device made by Rocket Medical Plc, listed in FDA GUDID since 23 Oct 2023 (UDI-DI 05055270979841), 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 Number05055270979841 UDI-DI Date23 Oct 2023ListedStatusListed 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  • Withdrawn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
Rocket
Generic name
Pleural catheter
Model / Ref / Catalog
R54701
Primary DI / UDI-DI
05055270979841
FDA product code
GBX
GMDN term
Pleural catheter
Device class
Class I
Regulation number
878.4200
GUDID distribution status
In Commercial Distribution

Related devices

Category: Pleural catheter

Similar devices in this category

Other devices filed under Pleural catheter.

Other devices from Rocket Medical Plc

See all devices from Rocket Medical Plc →

Properties

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