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SCANLAN® Vascu-Statt Appliers 9009-506A-10

by Scanlan International Inc

Ref 9009-506A-10

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

CE MDD

Valid until

Not listed

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

Registry data, not yet checked by deviCERTS. Source EUDAMED, GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD EUDAMED NumberB-00846159035155 Basic UDI-DI 00846159035155UDI-DIDate18 May 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00846159035155 UDI-DI Date22 Nov 2019ListedStatusListed 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.

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  • Withdrawn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
SCANLAN® Vascu-Statt Appliers
Generic Name
Surgical soft-tissue manipulation forceps, tweezers-like, reusable
Device Name
SCANLAN® CardioVasive™ Vascu‑Statt® Appliers
Model / Ref / Catalog
9009-506A-10
Description
CardioVasive™ Vascu Statt® Appliers (5 mm), Round Handle, Angled, (2.8 cm jaw length; 10 cm working length), 10 1/2" 27 cm
Primary DI / UDI-DI
00846159035155
Basic UDI-DI
B-00846159035155
FDA Product Code
GCJ
EMDN Code
L031306 Hemostatic forceps, reusable
GMDN Term
Surgical soft-tissue manipulation forceps, tweezers-like, reusable
Device Class
Class I EUDAMED
Class II GUDID
Regulation Number
876.1500
EU market of registration
Netherlands
GUDID distribution status
In Commercial Distribution
Sterilization Method
Moist Heat or Steam Sterilization

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device ClassEUDAMED
Class I
GUDID
Class II

Related devices

Category: Surgical soft-tissue manipulation forceps, tweezers-like, reusable

Other devices from Scanlan International Inc

See all devices from Scanlan International Inc →

Properties

  • Prescription Use
  • Premarket Exempt
  • Lot / Batch Number

Other properties (21)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Serial Number: No
  • Expiration Date: No
  • Manufacturing Date: No