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Aesculap PV008

by Aesculap AG

Part of a family of 175 devices: see the family page

Ref EX26203DEDZZAE

Aesculap PV008 is a Class I device made by Aesculap AG, registered in EUDAMED on 18 Jun 2026 (Basic UDI-DI 4995047MonitorEndoscopeG5) and listed in FDA GUDID since 7 May 2020 (UDI-DI 04046955206629), active as of 12 Nov 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 12 Nov 2026.

Regulatory status

as of registry sync 12 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number4995047MonitorEndoscopeG5 Basic UDI-DI 04046955206629UDI-DIDate18 Jun 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number04046955206629 UDI-DI Date7 May 2020ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 4995047MonitorEndoscopeG5 registered 18 Jun 2026 Active
  • FDA GUDID UDI-DI 04046955206629 listed 7 May 2020 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 04046955206629
  2. Registered EUDAMED 4995047MonitorEndoscopeG5

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  • Withdrawn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
EX2620-3D-Ae EUDAMED
Aesculap GUDID
Generic name
Endoscopic video image display unit
Device name
Endoscopic Monitor
Model / Ref / Catalog
EX26203DEDZZAE EUDAMED
PV008 GUDID
Primary DI / UDI-DI
04046955206629
Basic UDI-DI
4995047MonitorEndoscopeG5
FDA product code
KQM
EMDN code
Z11900802 Bioimaging viewing monitors
GMDN term
Endoscopic video image display unit
Device class
Class I
Regulation number
878.4160
EU registration type
Standard device
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Model / referenceEUDAMED
EX26203DEDZZAE
GUDID
PV008

Related devices

Category: Endoscopic video image display unit

Similar devices in this category

Other devices filed under BIOIMAGING VIEWING MONITORS.

Other devices from Aesculap AG

See all devices from Aesculap AG →

Properties

  • Prescription use
  • Premarket exempt
  • Serial number
Other properties (22, all answered No)