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Swathe

by Brownmed, Inc. 3 variants

Ref J50701Model Goliath

Swathe (J50701) is a Class I device made by Brownmed, Inc., registered in EUDAMED on 27 May 2026 (Basic UDI-DI 656480JSSWGOLNV), 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 Number656480JSSWGOLNV Basic UDI-DI 06564805070124UDI-DIDate27 May 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  • Withdrawn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
Joslin® Swathe
Model / reference
Goliath, J50701
Primary DI / UDI-DI
06564805070124
Basic UDI-DI
656480JSSWGOLNV
EMDN code
M030501 Immobilisation bandages for shoulder, arm and collarbone
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

Similar devices in this category

Other devices filed under IMMOBILISATION BANDAGES FOR SHOULDER, ARM AND COLLARBONE.

Other devices from Brownmed, Inc.

See all devices from Brownmed, Inc. →

Properties

Other properties (14, all answered No)