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Emprint CAPUMP1

by Covidien LP

Ref CAPUMP1

Emprint CAPUMP1 is a basic roller pump (EU MDR Class IIa; FDA Class II) made by Covidien LP, registered in EUDAMED on 16 Oct 2026 (Basic UDI-DI 0763000B00001026P) and listed in FDA GUDID since 24 Sep 2016 (UDI-DI 10884521190788), 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 Number0763000B00001026P Basic UDI-DI 10884521190788UDI-DIDate16 Oct 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number10884521190788 UDI-DI Date24 Sep 2016ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 0763000B00001026P registered 16 Oct 2026 Active
  • FDA GUDID UDI-DI 10884521190788 listed 24 Sep 2016 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 10884521190788
  2. Registered EUDAMED 0763000B00001026P

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  • Withdrawn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
Basic roller pump
Device name
Emprint™ Ablation Pump
Model / reference
CAPUMP1
Primary DI / UDI-DI
10884521190788
Basic UDI-DI
0763000B00001026P
FDA product code
NEY, GEI
EMDN code
L1899 Electrosurgery instruments, reusable - other
GMDN term
Basic roller pump
Device class
Class IIa 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 IIa
GUDID
Class II

Device class is stated on each registry's own scale: Class IIa 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: Basic roller pump

Similar devices in this category

Other devices filed under ELECTROSURGERY INSTRUMENTS, REUSABLE - OTHER.

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See all devices from Covidien LP →

Properties

  • Prescription use
  • Serial number
  • Manufacturing date
Other properties (22, all answered No)