Skip to content

Codman® 821731C

by Integra LifeSciences Production Corporation

Ref 82-1731C

Codman® 821731C (82-1731C) is a device classified as Class I in the EU and Class II in the US made by Integra LifeSciences Production Corporation, registered in EUDAMED on 16 Sep 2026 (Basic UDI-DI B-10381780518327) and listed in FDA GUDID since 28 Feb 2020 (UDI-DI 10381780518327), 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-10381780518327 Basic UDI-DI 10381780518327UDI-DIDate16 Sep 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number10381780518327 UDI-DI Date28 Feb 2020ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-10381780518327 registered 16 Sep 2026 Active
  • FDA GUDID UDI-DI 10381780518327 listed 28 Feb 2020 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 10381780518327
  2. Registered EUDAMED B-10381780518327

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  • Withdrawn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
Codman®
Generic name
Ventricular cerebrospinal fluid drainage catheterization kit
Model / Ref / Catalog
82-1731C, 821731C
Primary DI / UDI-DI
10381780518327
Basic UDI-DI
B-10381780518327
FDA product code
JXG
EMDN code
A060199 Surgical drainage systems - other
GMDN term
Ventricular cerebrospinal fluid drainage catheterization kit
Device class
Class I EUDAMED
Class II GUDID
Regulation number
882.5550
EU registration type
Legacy device (under a directive)
EU market of registration
Belgium
GUDID distribution status
In Commercial Distribution
MRI safety
MR Conditional

Truth per registry

2 sources · 2 fields differ

FieldEUDAMEDGUDID
Model / referenceEUDAMED
82-1731C
GUDID
821731C
Device classEUDAMED
Class I
GUDID
Class II

Device class is stated on each registry's own scale: Class I in the EU (EUDAMED), Class II in the US (FDA GUDID). EU and US classes are different schemes, so this is not a disagreement.

Related devices

Category: Ventricular cerebrospinal fluid drainage catheterization kit

Similar devices in this category

Other devices filed under SURGICAL DRAINAGE SYSTEMS - OTHER.

Other devices from Integra LifeSciences Production Corporation

See all devices from Integra LifeSciences Production Corporation →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (19, all answered No)