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neoprobe NPA76

by Devicor Medical Products, Inc.

Ref NPA76

neoprobe NPA76 is a hand-held-detector nuclear medicine system (EU MDR Class I; FDA Class I; FDA product code IZD, Probe, Uptake, Nuclear) made by Devicor Medical Products, Inc., registered in EUDAMED on 9 Jul 2026 (Basic UDI-DI 08419111AD03G000003322W3) and listed in FDA GUDID since 10 Nov 2016 (UDI-DI 00841911100249), active as of 22 Oct 2026.

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

CE MDR

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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number08419111AD03G000003322W3 Basic UDI-DI 00841911100249UDI-DIDate9 Jul 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00841911100249 UDI-DI Date10 Nov 2016ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 08419111AD03G000003322W3 registered 9 Jul 2026 Active
  • FDA GUDID UDI-DI 00841911100249 listed 10 Nov 2016 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 00841911100249
  2. Registered EUDAMED 08419111AD03G000003322W3

Coverage

2 jurisdictions

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  • Withdrawn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

Specification

EUDAMED · GUDID

Trade name
Neoprobe® Gamma Detection System EUDAMED
neoprobe GUDID
Generic name
Hand-held-detector nuclear medicine system
Device name
Probe cable
Model / Ref / Catalog
NPA76
Primary DI / UDI-DI
00841911100249
Basic UDI-DI
08419111AD03G000003322W3
FDA product code
IZD
EMDN code
Z129099 Various instruments for functional exploration and therapeutic interventions - other
GMDN term
Hand-held-detector nuclear medicine system
Device class
Class I
Regulation number
892.1320
EU registration type
Standard device
EU market of registration
Netherlands
GUDID distribution status
In Commercial Distribution

Related devices

Category: Hand-held-detector nuclear medicine system

Similar devices in this category

Other devices filed under VARIOUS INSTRUMENTS FOR FUNCTIONAL EXPLORATION AND THERAPEUTIC INTERVENTIONS - OTHER.

Other devices from Devicor Medical Products, Inc.

See all devices from Devicor Medical Products, Inc. →

Properties

  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (21, all answered No)