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Thd Self Bandy

by Thd S.P.A.

Ref 800341Model THD BANDY

Thd Self Bandy (800341) is a Class IIa device made by Thd S.P.A., registered in EUDAMED on 9 Sep 2026 (Basic UDI-DI 803373771BAN000237), 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 linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, synced 24 Oct 2026.

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number803373771BAN000237 Basic UDI-DI 08051887049295UDI-DIDate9 Sep 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Device name
Thd Light Bandy
Model / reference
THD BANDY, 800341
Primary DI / UDI-DI
08051887049295
Basic UDI-DI
803373771BAN000237
EMDN code
G020401 Haemorrhoid ligature sets
Device class
Class IIa
EU registration type
Standard device
EU market of registration
Italy

Manufacturer details

EUDAMED SRN
IT-MF-000029427

Similar devices in this category

Other devices filed under HAEMORRHOID LIGATURE SETS.

Other devices from Thd S.P.A.

See all devices from Thd S.P.A. →

Properties

Other properties (14, all answered No)