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SA-M MultiPad

by Brownmed, Inc.

Ref 71372Model Medium

SA-M MultiPad (71372) is a Class I device made by Brownmed, Inc., registered in EUDAMED on 1 Jun 2026 (Basic UDI-DI 082161SOSTSAMD713Z6), 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, self-declared

Class I: no certifier involved

Trust

Unverified

Source EUDAMED, synced 25 Oct 2026.

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number082161SOSTSAMD713Z6 Basic UDI-DI 00821617137220UDI-DIDate1 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  • Withdrawn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

Device name
Soft Stride™ SA-M MultiPad
Model / reference
Medium, 71372
Primary DI / UDI-DI
00821617137220
Basic UDI-DI
082161SOSTSAMD713Z6
EMDN code
Y061203 Orthoses, foot (including insoles and inserts)
Device class
Class I
EU registration type
Standard device
EU market of registration
Netherlands

Manufacturer details

EUDAMED SRN
US-MF-000008271
Authorised representative
AR Experts B.V. NL-AR-000023989

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Other devices filed under ORTHOSES, FOOT (INCLUDING INSOLES AND INSERTS).

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Properties

Other properties (14, all answered No)