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Lunar V1

by GE Medical Systems Ultrasound and Primary Care Diagnostics LLC

Ref LU50015Model Lunar Astra

Lunar V1 (LU50015) is a Class IIb device made by GE Medical Systems Ultrasound and Primary Care Diagnostics LLC, registered in EUDAMED on 4 Sep 2026 (Basic UDI-DI 8406821BUG00385HV), 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 linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, synced 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number8406821BUG00385HV Basic UDI-DI 00198953052679UDI-DIDate4 Sep 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device name
Lunar Astra
Model / reference
Lunar Astra, LU50015
Primary DI / UDI-DI
00198953052679
Basic UDI-DI
8406821BUG00385HV
EMDN code
Z11900103 X–ray bone densitometers
Device class
Class IIb
System or procedure pack
System which is a device in itself
EU registration type
Standard device
EU market of registration
France

Manufacturer details

EUDAMED SRN
US-MF-000016664
Authorised representative
GE Medical Systems SCS FR-AR-000000344

Similar devices in this category

Other devices filed under BONE DENSITOMETRY SYSTEMS.

Other devices from GE Medical Systems Ultrasound and Primary Care Diagnostics LLC

See all devices from GE Medical Systems Ultrasound and Primary Care Diagnostics LLC →

Properties

  • Measuring function
Other properties (13, all answered No)