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Polypectomy Snare

by Anrei Medical (Hangzhou) Co., Ltd. 83 variants

Ref SNESCMW824

Polypectomy Snare (SNESCMW824) is a Class IIb device made by Anrei Medical (Hangzhou) Co., Ltd., registered in EUDAMED on 30 Oct 2026 (Basic UDI-DI B-06948318997084), active as of 7 Nov 2026.

Active European Union

CE MDD

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 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-06948318997084 Basic UDI-DI Date30 Oct 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Active

Specification

EUDAMED

Device name
Polypectomy Snare
Model / reference
SNESCMW824
Primary DI / UDI-DI
06948318997084, 06926839800489
Basic UDI-DI
B-06948318997084, B-06926839800489
EMDN code
G03030102 Polypectomy snares, non-revolving
Device class
Class IIb
EU registration type
Legacy device (under a directive)
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
CN-MF-000009964
Authorised representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Similar devices in this category

Other devices filed under POLYPECTOMY SNARES, NON-REVOLVING.

Other devices from Anrei Medical (Hangzhou) Co., Ltd.

See all devices from Anrei Medical (Hangzhou) Co., Ltd. →

Properties

  • Supplied sterile
Other properties (11, all answered No)