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Interlock™-35 M001363590

by Boston Scientific

Ref M001363590

Interlock™-35 M001363590 is a device classified as Class IIb in the EU and Class II in the US made by Boston Scientific, registered in EUDAMED on 12 Oct 2026 (Basic UDI-DI B-08714729793014) and listed in FDA GUDID since 24 Sep 2015 (UDI-DI 08714729793014), active as of 24 Oct 2026.

Active European Union. Also listed in GUDID (US).

CE MDD

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, GUDID, synced 24 Oct 2026.

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD EUDAMED NumberB-08714729793014 Basic UDI-DI 08714729793014UDI-DIDate12 Oct 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number08714729793014 UDI-DI Date24 Sep 2015ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-08714729793014 registered 12 Oct 2026 Active
  • FDA GUDID UDI-DI 08714729793014 listed 24 Sep 2015 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 08714729793014
  2. Registered EUDAMED B-08714729793014

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDD Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Trade name
Interlock™ EUDAMED
Interlock™-35 GUDID
Generic name
Non-neurovascular embolization coil
Model / Ref / Catalog
M001363590
Primary DI / UDI-DI
08714729793014
Basic UDI-DI
B-08714729793014
FDA product code
KRD
EMDN code
C010402020301 Embolisation coils
GMDN term
Non-neurovascular embolization coil
Device class
Class IIb EUDAMED
Class II GUDID
Regulation number
870.3300
System or procedure pack
System which is a device in itself
EU registration type
Legacy device (under a directive)
EU market of registration
Netherlands
GUDID distribution status
In Commercial Distribution
MRI safety
MR Conditional

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device classEUDAMED
Class IIb
GUDID
Class II

Related devices

Category: Non-neurovascular embolization coil

Other devices from Boston Scientific

See all devices from Boston Scientific →

Properties

  • Supplied sterile
  • Single use
  • Implantable
  • Contains animal tissues or cells
  • Prescription use
  • Convenience kit
  • Lot / batch number
  • Expiration date
Other properties (17, all answered No)