Skip to content

Emprint CART1

by Covidien LP

Ref CART1

Emprint CART1 is an electromechanical device/system transport trolley (EU MDR Class I; FDA Class II; FDA product code NEY, System, Ablation, Microwave and Accessories) made by Covidien LP, registered in EUDAMED on 16 Oct 2026 (Basic UDI-DI 0763000B00008568H) and listed in FDA GUDID since 24 Dec 2020 (UDI-DI 10884521203006), active as of 24 Oct 2026.

Active European Union. Also listed in GUDID (US).

CE MDR

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, GUDID, synced 24 Oct 2026.

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number0763000B00008568H Basic UDI-DI 10884521203006UDI-DIDate16 Oct 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number10884521203006 UDI-DI Date24 Dec 2020ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 0763000B00008568H registered 16 Oct 2026 Active
  • FDA GUDID UDI-DI 10884521203006 listed 24 Dec 2020 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 10884521203006
  2. Registered EUDAMED 0763000B00008568H

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDR Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Trade name
Emprint™ EUDAMED
Emprint GUDID
Generic name
Electromechanical device/system transport trolley
Device name
HP Ablation Cart
Model / reference
CART1
Primary DI / UDI-DI
10884521203006
Basic UDI-DI
0763000B00008568H
FDA product code
NEY
EMDN code
L1899 Electrosurgery instruments, reusable - other
GMDN term
Electromechanical device/system transport trolley
Device class
Class I EUDAMED
Class II GUDID
Regulation number
878.4400
EU registration type
Standard device
EU market of registration
Netherlands
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device classEUDAMED
Class I
GUDID
Class II

Device class is stated on each registry's own scale: Class I in the EU (EUDAMED), Class II in the US (FDA GUDID). EU and US classes are different schemes, so this is not a disagreement.

Related devices

Category: Electromechanical device/system transport trolley

Similar devices in this category

Other devices filed under ELECTROSURGERY INSTRUMENTS, REUSABLE - OTHER.

Other devices from Covidien LP

  • LigaSure MRASILF19

    Class II

  • Shiley 110860

    Class II

  • Shiley 110865

    Class II

  • Shiley 110870

    Class II

See all devices from Covidien LP →

Properties

  • Prescription use
  • Lot / batch number
  • Manufacturing date
Other properties (22, all answered No)