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PVA Packing

by Invotec International, Inc. 5 variants

Part of a family of 20 devices: see the family page

Ref 22-60110FModel PVA Packing

PVA Packing (22-60110F) is a Class I device made by Invotec International, Inc., registered in EUDAMED on 26 May 2026 (Basic UDI-DI 081850102PVAPackingYA), active as of 25 Oct 2026.

Active European Union

CE MDR

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, synced 25 Oct 2026.

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number081850102PVAPackingYA Basic UDI-DI 00818501022786UDI-DIDate26 May 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Device name
PVA Packing
Model / reference
PVA Packing, 22-60110F
Primary DI / UDI-DI
00818501022786
Basic UDI-DI
081850102PVAPackingYA
EMDN code
Q0399 ENT devices - other
Device class
Class I
EU registration type
Standard device
EU market of registration
Austria

Manufacturer details

EUDAMED SRN
US-MF-000024855
Authorised representative
MDSS GmbH DE-AR-000005430

Similar devices in this category

Other devices filed under ENT DEVICES - OTHER.

Other devices from Invotec International, Inc.

See all devices from Invotec International, Inc. →

Properties

  • Supplied sterile
Other properties (13, all answered No)