Skip to content

Hall® Titan™

by Conmed Corporation 3 variants

Ref PRO9450B, PRO9200B, PRO9100B, PRO9270-2B, PRO9400B

Active European Union. Also listed in GUDID (US), partly in commercial distribution.

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 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD EUDAMED NumberB-40845854050829 Basic UDI-DI Date8 Apr 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number40845854050829 UDI-DI Date30 Jun 2020ListedStatusListed GUDID: 4 of 5 UDI-DIs 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  • Withdrawn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

Generic Name
Bone/joint surgical power tool motorized handpiece/set, electric, reusable
Device Name
Orthopedic, Active, Handpiece, Battery, Pistol-grip, All, Hall Titan, Saws
Orthopedic, Active, Handpiece, Battery, Pistol-grip, All, Hall Titan, Modular
Model / Ref / Catalog
PRO9450B, PRO9200B, PRO9100B, PRO9270-2B, PRO9400B
Primary DI / UDI-DI
40845854050829, 40845854050836, 40845854050775, 30653405990745, 40845854050812
Basic UDI-DI
B-40845854050829, B-40845854050836, B-40845854050775, B-30653405990745, B-40845854050812
FDA Product Code
HAB
EMDN Code
Z12130502, Z12130503
GMDN Term
Bone/joint surgical power tool motorized handpiece/set, electric, reusable
Device Class
Class IIa EUDAMED
Class I GUDID
Regulation Number
878.4820
EU market of registration
Belgium
GUDID distribution status
In Commercial Distribution (UDI-DI 40845854050836, 40845854050775, 40845854050829, 30653405990745)
Not in Commercial Distribution (UDI-DI 40845854050812)
Sterilization Method
Moist Heat or Steam Sterilization

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device ClassEUDAMED
Class IIa
GUDID
Class I

Manufacturer details

EUDAMED SRN
US-MF-000012663
Authorised representative
MDSS GmbH DE-AR-000005430

Other devices from Conmed Corporation

See all devices from Conmed Corporation →

Properties

  • Prescription Use
  • Premarket Exempt
  • Serial Number
  • Manufacturing Date

Other properties (20)

  • 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
  • Lot / Batch Number: No
  • Expiration Date: No