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Pivot-Points

by devemed GmbH 9 variants

Ref 675-22

Pivot-Points (675-22) is a Class I device made by devemed GmbH, registered in EUDAMED on 14 Jul 2026 (Basic UDI-DI 4061644PG08010445), 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 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/MDR Number4061644PG08010445 Basic UDI-DI 04061644031917UDI-DIDate14 Jul 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device name
Pivot-Points
Model / reference
675-22
Primary DI / UDI-DI
04061644031917
Basic UDI-DI
4061644PG08010445
Direct marketing DI
04061644031917
EMDN code
L99 Surgical instruments, reusable - other
Device class
Class I
EU registration type
Standard device
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
DE-MF-000005568

Similar devices in this category

Other devices filed under SURGICAL INSTRUMENTS, REUSABLE - OTHER.

Other devices from devemed GmbH

See all devices from devemed GmbH →

Properties

  • Sterilise before use
  • Reusable
Other properties (12, all answered No)