Skip to content

Blayco-Pad

by Telic, S.A.U.

Ref AC-3020

Blayco-Pad (AC-3020) is a Class I device made by Telic, S.A.U., registered in EUDAMED on 8 Aug 2024 (Basic UDI-DI 8427734PROTECTIVEPADY2), 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, self-declared

Class I: no certifier involved

Trust

Unverified

Source EUDAMED, synced 25 Oct 2026.

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number8427734PROTECTIVEPADY2 Basic UDI-DI 08427734001028UDI-DIDate8 Aug 2024RegisteredStatusActive

Official records

Certificates

0 certificates · EUDAMED

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

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device name
Protective pad
Model / reference
AC-3020
Primary DI / UDI-DI
08427734001028
Basic UDI-DI
8427734PROTECTIVEPADY2
EMDN code
T0306 Patient protection devices during clinical procedures
Device class
Class I
EU registration type
Standard device
EU market of registration
Spain

Manufacturer details

EUDAMED SRN
ES-MF-000001853

Related devices

Category: Radiation/mechanical corneal shield, reusable

Similar devices in this category

Other devices filed under PATIENT PROTECTION DEVICES DURING CLINICAL PROCEDURES.

Other devices from Telic, S.A.U.

See all devices from Telic, S.A.U. →

Properties

Other properties (14, all answered No)