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Penumbra System APCAN2

by Penumbra, Inc.

Ref APCAN2Model Non-Sterile Pump MAX Supplies – Artemis

Penumbra System APCAN2 is a device classified as Class I in the EU and Class II in the US made by Penumbra, Inc., registered in EUDAMED on 26 May 2026 (Basic UDI-DI 081454801ARTSUPBD), cleared under FDA 510(k) K051758 on 17 Aug 2005 and listed in FDA GUDID since 2 Oct 2017 (UDI-DI 00810169721841), active as of 22 Oct 2026.

Active European Union and United States. Also listed in GUDID (US).

CE MDR 510(k)

Valid until

No date given

CE: no date in EUDAMED. FDA: not time-limited

FDA recalls

None found

in data synced 22 Oct 2026

Documents

None, self-declared

Class I: no certifier involved

510(k) K051758

FDA submission, from GUDID

Trust

Unverified

Source EUDAMED, GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number081454801ARTSUPBD Basic UDI-DI 00810169721841UDI-DIDate26 May 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00810169721841 UDI-DI Date2 Oct 2017ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE GUDID from GUDID Substantially Equivalent · Traditional NumberK051758 Date17 Aug 2005DecidedStatusActive

Official records

Across registries

3 registries list this device

  • EUDAMED Basic UDI-DI 081454801ARTSUPBD registered 26 May 2026 Active
  • FDA 510(k) K051758 decided 17 Aug 2005 Active
  • FDA GUDID UDI-DI 00810169721841 listed 2 Oct 2017 Listed

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Timeline

3 dated events

  1. Cleared FDA 510(k) K051758
  2. Listed FDA GUDID 00810169721841
  3. Registered EUDAMED 081454801ARTSUPBD

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDR Active
  • United States FDA 510(k) Active

Specification

EUDAMED · GUDID

Trade name
Non-Sterile Pump MAX Supplies – Artemis EUDAMED
Penumbra System GUDID
Generic name
Surgical irrigation/aspiration system
Device name
Pump MAX Canister
Model / reference
APCAN2, Non-Sterile Pump MAX Supplies – Artemis
Primary DI / UDI-DI
00810169721841 EUDAMED
00814548017952 GUDID
Basic UDI-DI
081454801ARTSUPBD
510(k) Number
FDA product code
JCX
EMDN code
A060199 Surgical drainage systems - other
GMDN term
Surgical irrigation/aspiration system
Device class
Class I EUDAMED
Class II GUDID
Regulation number
878.4780
EU registration type
Standard device
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 2 fields differ

FieldEUDAMEDGUDID
Primary DI / UDI-DIEUDAMED
00810169721841
GUDID
00814548017952
Device classEUDAMED
Class I
GUDID
Class II

The registries describe this device under different primary UDI-DIs (EUDAMED lists 00810169721841; FDA GUDID lists 00814548017952), so their flags are not compared. 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: Surgical irrigation/aspiration system

Cleared under the same submission (K051758)

Similar devices in this category

Other devices filed under SURGICAL DRAINAGE SYSTEMS - OTHER.

Other devices from Penumbra, Inc.

See all devices from Penumbra, Inc. →

Properties

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