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SeQureTM Snare System LT-SP-10

by Lifetech Scientific (Shenzhen) Co., Ltd.

Ref LT-SP-10

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

CE MDD

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

None found

in data synced 22 Oct 2026

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

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

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD EUDAMED NumberB-06938370118084 Basic UDI-DI 06938370118084UDI-DIDate15 Dec 2022RegisteredStatusActive
United StatesGUDID listing GUDID Number06938370118084 UDI-DI Date17 Nov 2017ListedStatusListed GUDID: in commercial distribution

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 22 Oct 2026.

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  • Withdrawn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
SeQure EUDAMED
SeQureTM Snare System GUDID
Generic Name
Intravascular extraction catheter-snare
Device Name
SeQure™ Snare System
Model / Reference
LT-SP-10
Primary DI / UDI-DI
06938370118084
Basic UDI-DI
B-06938370118084
510(k) Number
FDA Product Code
MMX
EMDN Code
C019005 Retrieving systems for vascular foreign bodies
GMDN Term
Intravascular extraction catheter-snare
Device Class
Class IIa EUDAMED
Class II GUDID
Regulation Number
870.5150
EU market of registration
France
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device ClassEUDAMED
Class IIa
GUDID
Class II

Related devices

Cleared under the same submission (K102484)

Other devices from Lifetech Scientific (Shenzhen) Co., Ltd.

See all devices from Lifetech Scientific (Shenzhen) Co., Ltd. →

Properties

  • Sterile
  • Single Use
  • Prescription Use
  • Lot / Batch Number
  • Serial Number
  • Expiration Date
  • Manufacturing Date

Other properties (15)

  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No