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ReadyWrap

by L&R USA Inc.

Ref 401342Model ReadyWrap

ReadyWrap (401342) is a Class I device made by L&R USA Inc., registered in EUDAMED on 25 Jun 2026 (Basic UDI-DI 081264502-RA.003.012-ZT), active as of 24 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 24 Oct 2026.

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number081264502-RA.003.012-ZT Basic UDI-DI 00810173923453UDI-DIDate25 Jun 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  • Withdrawn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

Model / reference
ReadyWrap, 401342
Primary DI / UDI-DI
00810173923453
Basic UDI-DI
081264502-RA.003.012-ZT
EMDN code
M030499 Elastic bandages, support and compression - other
Device class
Class I
EU registration type
Standard device
EU market of registration
Austria

Manufacturer details

EUDAMED SRN
US-MF-000053106
Authorised representative
Emergo Europe B.V. NL-AR-000000116

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Properties

Other properties (14, all answered No)