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PDT, Inc. R226 Explorer/Probe 23/UNC-15

by PDT, Inc.

Part of a family of 34 devices: see the family page

Ref R226Model Diagnostic Family

PDT, Inc. R226 Explorer/Probe 23/UNC-15 is a dental surgical probe (EU MDR Class I; FDA Class I) made by PDT, Inc., registered in EUDAMED on 4 Nov 2026 (Basic UDI-DI 0813677021802WE) and listed in FDA GUDID since 30 Apr 2021 (UDI-DI 00813677021366), active as of 7 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 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number0813677021802WE Basic UDI-DI 00813677021366UDI-DIDate4 Nov 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00813677021366 UDI-DI Date30 Apr 2021ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 0813677021802WE registered 4 Nov 2026 Active
  • FDA GUDID UDI-DI 00813677021366 listed 30 Apr 2021 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 00813677021366
  2. Registered EUDAMED 0813677021802WE

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  • Withdrawn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
Explorer 23 -Probe UNC15 EUDAMED
PDT, Inc. GUDID
Generic name
Dental surgical probe, reusable
Device name
Dental Probes and Explorers
Model / Ref / Catalog
Diagnostic Family, R226, R226 Explorer/Probe 23/UNC-15
Primary DI / UDI-DI
00813677021366
Basic UDI-DI
0813677021802WE
Direct marketing DI
00813677021366
FDA product code
EKB, EIX
EMDN code
L159003 Dental and periodontal probes and explorers, reusable
GMDN term
Dental surgical probe, reusable
Device class
Class I
Regulation number
872.4565
EU registration type
Standard device
EU market of registration
Austria
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Model / referenceEUDAMED
Diagnostic Family
R226
GUDID
R226 Explorer/Probe 23/UNC-15

Related devices

Category: Dental surgical probe, reusable

Similar devices in this category

Other devices filed under DENTAL AND PERIODONTAL PROBES AND EXPLORERS, REUSABLE.

Other devices from PDT, Inc.

See all devices from PDT, Inc. →

Properties

  • Sterilise before use
  • Premarket exempt
Other properties (23, all answered No)