Skip to content

MESA® Spinal System

by K2M, Inc. 96 variants

Part of a family of 141 devices: see the family page

Ref 801-90071Model 08858251001823SX

MESA® Spinal System (801-90071) is a Class I device made by K2M, Inc., registered in EUDAMED on 28 Oct 2026 (Basic UDI-DI 08858251001823SX), active as of 7 Nov 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 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number08858251001823SX Basic UDI-DI 10888857472693UDI-DIDate28 Oct 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  • Withdrawn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
Mesa Container
Model / reference
08858251001823SX, 801-90071
Primary DI / UDI-DI
10888857472693
Basic UDI-DI
08858251001823SX
Direct marketing DI
10888857472693
EMDN code
V0402 Clinical use trays and bowls
Device class
Class I
EU registration type
Standard device
EU market of registration
Netherlands

Manufacturer details

EUDAMED SRN
US-MF-000004440
Authorised representative
Emergo Europe B.V. NL-AR-000000116

Similar devices in this category

Other devices filed under CLINICAL USE TRAYS AND BOWLS.

Other devices from K2M, Inc.

See all devices from K2M, Inc. →

Properties

  • Sterilise before use
Other properties (13, all answered No)