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Mayfield®

by Integra Lifesciences Corporation 2 variants

Part of a family of 24 devices: see the family page

Ref A2102

Mayfield® (A2102) is a Class I device made by Integra Lifesciences Corp., registered in EUDAMED on 6 Jul 2026 (Basic UDI-DI 038178B0040CSS2E), active as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number038178B0040CSS2E Basic UDI-DI 10381780268024UDI-DIDate6 Jul 2026RegisteredStatusActive

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  • Withdrawn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
Mayfield Base Units and Adaptors
Model / reference
A2102
Primary DI / UDI-DI
10381780268024
Basic UDI-DI
038178B0040CSS2E
Direct marketing DI
10381780268024
EMDN code
Z12011280 Patient positioning instruments - hardware accessories
Device class
Class I
EU registration type
Standard device
EU market of registration
Belgium

Manufacturer details

EUDAMED SRN
US-MF-000025259
Authorised representative
Integra LifeSciences Services FR-AR-000002474

Similar devices in this category

Other devices filed under PATIENT POSITIONING INSTRUMENTS - HARDWARE ACCESSORIES.

Other devices from Integra Lifesciences Corp.

See all devices from Integra Lifesciences Corp. →

Properties

Other properties (14, all answered No)