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Popple

by Aspen Medical Products, LLC 6 variants

Part of a family of 170 devices: see the family page

Ref PPL373

Popple (PPL373) is a Class I device made by Aspen Medical Products, LLC, registered in EUDAMED on 8 Aug 2025 (Basic UDI-DI 081824901LSOH8), active as of 23 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number081824901LSOH8 Basic UDI-DI 00818249016979UDI-DIDate8 Aug 2025RegisteredStatusActive

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  • Withdrawn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
Lumbar
Model / reference
PPL373
Primary DI / UDI-DI
00818249016979
Basic UDI-DI
081824901LSOH8
EMDN code
Y060308 Lumbosacral spine orthoses
Device class
Class I
EU registration type
Standard device
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
US-MF-000001571
Authorised representative
Emergo Europe B.V. NL-AR-000000116

Similar devices in this category

Other devices filed under LUMBOSACRAL SPINE ORTHOSES.

Other devices from Aspen Medical Products, LLC

See all devices from Aspen Medical Products, LLC →

Properties

Other properties (14, all answered No)