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Ankle, Heel & Foot Orthosis Brace

by Fortune Company Limited 7 variants

Ref A01-S2Model A01-S2,A01-L2,A02-SM,A02-MD,A02-LG,A02-XL,A03b-S2,A03b-L2,A04-UN,A06-UN,A08-UN,A08-SM,A08-MD,A08-LG,A09-UN,A09-S2,A09-L2,A10-UN,A11-SM-LT,A11-MD-LT,A11-LG-LT,A11-XL-LT,A11-SM-RT,A11-MD-RT,A11-LG-RT,A11-XL-RT, etc.

Active European Union

CE MDR

Valid until

Not listed

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

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number698005810AHFOBC3 Basic UDI-DI 06980058100720UDI-DIDate13 Jul 2026RegisteredStatusActive

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  • Withdrawn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
Ankle, Heel & Foot Orthosis Brace
Model / Reference
A01-S2, A01-L2, A02-SM, A02-MD, A02-LG, A02-XL, A03b-S2, A03b-L2, A04-UN, A06-UN, A08-UN, A08-SM, A08-MD, A08-LG, A09-UN, A09-S2, A09-L2, A10-UN, A11-SM-LT, A11-MD-LT, A11-LG-LT, A11-XL-LT, A11-SM-RT, A11-MD-RT, A11-LG-RT, A11-XL-RT, etc.
Primary DI / UDI-DI
06980058100720
Basic UDI-DI
698005810AHFOBC3
EMDN Code
Y061203 Orthoses, foot (including insoles and inserts)
Device Class
Class I
EU market of registration
Austria

Manufacturer details

EUDAMED SRN
CN-MF-000023028
Authorised representative
SUNGO Europe B.V. NL-AR-000000247

Other devices from Fortune Company Ltd.

See all devices from Fortune Company Ltd. →

Properties

Other properties (13)

  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No