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Iso Gard Filter a

by Teleflex Medical Sdn. Bhd.

Ref 18212Model IPN929898

Iso Gard Filter a (18212) is a Class IIa device made by Teleflex Medical Sdn. Bhd., registered in EUDAMED on 31 Jul 2026 (Basic UDI-DI B-04026704347940), active as of 25 Oct 2026.

Active European Union

CE MDD

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/MDD NumberB-04026704347940 Basic UDI-DI Date31 Jul 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Active

Specification

EUDAMED

Device name
Iso-Gard Filter Angled
Model / reference
18212, IPN929898
Primary DI / UDI-DI
04026704347940, 14026704927699
Basic UDI-DI
B-04026704347940, B-14026704927699
EMDN code
R040101 Antibacterial and antiviral respiratory filters
Device class
Class IIa
EU registration type
Legacy device (under a directive)
EU market of registration
Ireland

Manufacturer details

EUDAMED SRN
MY-MF-000024692
Authorised representative
Teleflex Medical IE-AR-000015869

Similar devices in this category

Other devices filed under ANTIBACTERIAL AND ANTIVIRAL RESPIRATORY FILTERS.

Other devices from Teleflex Medical Sdn. Bhd.

See all devices from Teleflex Medical Sdn. Bhd. →

Properties

Other properties (14, all answered No)