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Mayfield® A1023

by Integra Lifesciences Corp.

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

Ref A1023

Mayfield® A1023 is a Class I device made by Integra Lifesciences Corp., registered in EUDAMED on 6 Jul 2026 (Basic UDI-DI 038178B0040CSS2E) and listed in FDA GUDID since 10 Apr 2018 (UDI-DI 10381780267546), active as of 25 Oct 2026.

Active European Union. Also listed in GUDID (US).

CE MDR

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, GUDID, synced 25 Oct 2026.

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number038178B0040CSS2E Basic UDI-DI 10381780267546UDI-DIDate6 Jul 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number10381780267546 UDI-DI Date10 Apr 2018ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 038178B0040CSS2E registered 6 Jul 2026 Active
  • FDA GUDID UDI-DI 10381780267546 listed 10 Apr 2018 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 10381780267546
  2. Registered EUDAMED 038178B0040CSS2E

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDR Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Trade name
Mayfield®
Generic name
Medical table clamp
Device name
Mayfield Base Units and Adaptors
Model / Ref / Catalog
A1023
Primary DI / UDI-DI
10381780267546
Basic UDI-DI
038178B0040CSS2E
Direct marketing DI
10381780267546
FDA product code
FWZ
EMDN code
Z12011280 Patient positioning instruments - hardware accessories
GMDN term
Medical table clamp
Device class
Class I
Regulation number
878.4950
EU registration type
Standard device
EU market of registration
Belgium
GUDID distribution status
In Commercial Distribution
MRI safety
MR Unsafe

Related devices

Category: Medical table clamp

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

  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Serial number
  • Manufacturing date
Other properties (20, all answered No)