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ExtriCARE MI392-0001

by Alleva Medical Limited

Ref MI392

ExtriCARE MI392-0001 (EC3600-1000C-E) is a negative-pressure wound therapy system canister (EU MDR Class IIa; FDA Class II; FDA product code OMP, Negative Pressure Wound Therapy Powered Suction Pump) made by Alleva Medical Limited, registered in EUDAMED on 1 Jul 2026 (Basic UDI-DI 489708907MI392KQ), cleared under FDA 510(k) K143362 on 3 Feb 2015 and listed in FDA GUDID since 12 Dec 2023 (UDI-DI 04897089070040), active as of 12 Nov 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 12 Nov 2026

Documents

None linked in EUDAMED

A group certificate may exist

510(k) K143362

FDA submission, from GUDID

Trust

Unverified

Source EUDAMED, GUDID, synced 12 Nov 2026.

Regulatory status

as of registry sync 12 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number489708907MI392KQ Basic UDI-DI 04897089070040UDI-DIDate1 Jul 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number04897089070040 UDI-DI Date12 Dec 2023ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE GUDID from GUDID Substantially Equivalent · Special NumberK143362 Date3 Feb 2015DecidedStatusActive

Official records

Across registries

3 registries list this device

  • EUDAMED Basic UDI-DI 489708907MI392KQ registered 1 Jul 2026 Active
  • FDA 510(k) K143362 decided 3 Feb 2015 Active
  • FDA GUDID UDI-DI 04897089070040 listed 12 Dec 2023 Listed

Timeline

3 dated events

  1. Cleared FDA 510(k) K143362
  2. Listed FDA GUDID 04897089070040
  3. Registered EUDAMED 489708907MI392KQ

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  • Withdrawn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
extriCARE® 3600 Negative Pressure Wound Therapy Pump 1000cc Canister EUDAMED
ExtriCARE GUDID
Generic name
Negative-pressure wound therapy system canister
Model / Ref / Catalog
MI392 EUDAMED
MI392-0001 GUDID
EC3600-1000C-E GUDID
Primary DI / UDI-DI
04897089070040
Basic UDI-DI
489708907MI392KQ
Direct marketing DI
04897089070040
510(k) Number
FDA product code
OMP
EMDN code
Z12019003 Wound treatment equipment
GMDN term
Negative-pressure wound therapy system canister
Device class
Class IIa 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
Model / referenceEUDAMED
MI392
GUDID
MI392-0001
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: Negative-pressure wound therapy system canister

Similar devices in this category

Other devices filed under WOUND TREATMENT EQUIPMENT.

Other devices from Alleva Medical Limited

See all devices from Alleva Medical Limited →

Properties

  • Single use
  • Prescription use
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (20, all answered No)