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ClearChart4P 13785

by Reichert Inc.

Ref 13785AG, 13785SE, 13785DLModel 13795

ClearChart4P 13785 is a Class I device made by Reichert Inc., registered in EUDAMED on 23 Feb 2026 (Basic UDI-DI 081255901CLC001T3) and listed in FDA GUDID since 12 Aug 2025 (UDI-DI 00812559012232), active as of 25 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 25 Oct 2026.

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number081255901CLC001T3 Basic UDI-DI 00812559012232UDI-DIDate23 Feb 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00812559012232 UDI-DI Date12 Aug 2025ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 081255901CLC001T3 registered 23 Feb 2026 Active
  • FDA GUDID UDI-DI 00812559012232 listed 12 Aug 2025 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 00812559012232
  2. Registered EUDAMED 081255901CLC001T3

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  • Withdrawn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
ClearChart® 4P EUDAMED
ClearChart4P GUDID
Generic name
Vision testing/training chart
Device name
ClearChart® 4
Model / reference
13795 EUDAMED
13785AG EUDAMED
13785SE EUDAMED
13785DL EUDAMED
13785 GUDID
Primary DI / UDI-DI
00812559012232
Basic UDI-DI
081255901CLC001T3
FDA product code
HOX
EMDN code
Z1212012001 Visual functional assessment equipment
GMDN term
Vision testing/training chart
Device class
Class I
Regulation number
886.1150
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
13795
13785AG, 13785SE, 13785DL
GUDID
13785

Related devices

Category: Vision testing/training chart

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Other devices filed under VISUAL FUNCTIONAL ASSESSMENT EQUIPMENT.

Other devices from Reichert Inc.

See all devices from Reichert Inc. →

Properties

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