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Drypro Model 832 Gnpm

by Konica Minolta, Inc.

Model DRYPRO MODEL 832

Drypro Model 832 Gnpm is a device classified as Class I in the EU and Class II in the US made by Konica Minolta, Inc., registered in EUDAMED on 21 Apr 2025 (Basic UDI-DI 45601419200000583), cleared under FDA 510(k) K061999 on 15 Aug 2006 and listed in FDA GUDID since 19 Sep 2016 (UDI-DI 04560141922686), active as of 23 Oct 2026.

Active European Union and United States. Also listed in GUDID (US).

CE MDR 510(k)

Valid until

No date given

CE: no date in EUDAMED. FDA: not time-limited

FDA recalls

None found

in data synced 23 Oct 2026

Documents

None linked in EUDAMED

A group certificate may exist

510(k) K061999

FDA submission, from GUDID

Trust

Unverified

Source EUDAMED, GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number45601419200000583 Basic UDI-DI 04560141922686UDI-DIDate21 Apr 2025RegisteredStatusActive
United StatesGUDID listing GUDID Number04560141922686 UDI-DI Date19 Sep 2016ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE GUDID from GUDID Substantially Equivalent · Traditional NumberK061999 Date15 Aug 2006DecidedStatusActive

Official records

Across registries

3 registries list this device

  • EUDAMED Basic UDI-DI 45601419200000583 registered 21 Apr 2025 Active
  • FDA 510(k) K061999 decided 15 Aug 2006 Active
  • FDA GUDID UDI-DI 04560141922686 listed 19 Sep 2016 Listed

Timeline

3 dated events

  1. Cleared FDA 510(k) K061999
  2. Listed FDA GUDID 04560141922686
  3. Registered EUDAMED 45601419200000583

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDR Active
  • United States FDA 510(k) Active

Specification

EUDAMED · GUDID

Trade name
Drypro Model 832
Generic name
Diagnostic-imaging multiformat camera
Model / reference
DRYPRO MODEL 832 EUDAMED
GNPM GUDID
Primary DI / UDI-DI
04560141922686
Basic UDI-DI
45601419200000583
Direct marketing DI
04560141922686
510(k) Number
FDA product code
LMC
EMDN code
Z110705 Laser imagers for bioimaging
GMDN term
Diagnostic-imaging multiformat camera
Device class
Class I EUDAMED
Class II GUDID
Regulation number
892.2040
EU registration type
Standard device
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution
MRI safety
MR Unsafe

Truth per registry

2 sources · 2 fields differ

FieldEUDAMEDGUDID
Model / referenceEUDAMED
DRYPRO MODEL 832
GUDID
GNPM
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: Diagnostic-imaging multiformat camera

Cleared under the same submission (K061999)

Similar devices in this category

Other devices filed under X–RAY FILM IMAGING SUPPORT INSTRUMENTS.

Other devices from Konica Minolta, Inc.

See all devices from Konica Minolta, Inc. →

Properties

  • Prescription use
  • Serial number
Other properties (23, all answered No)