← Back to catalogue

IS 3600 I/O 3D Scanner

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 6568745Ref 1.014.6109

by Dental Imaging Technologies Corporation

Identity

Trade Name
IS 3600 I/O 3D Scanner EUDAMEDFDA UDI
DEXIS IXS Size 2 Accessory Layer EUDAMED
Generic Name
Intraoral optical scanning system FDA UDI
Device Name
IS 3600 I/O 3D Scanner EUDAMED
Intraoral Positioning System EUDAMED
Model / Reference
6568745 EUDAMEDFDA UDI
1.014.6109 EUDAMED

Identifiers

Catalog Number
6568745 FDA UDI
Primary DI / UDI-DI
00693856000005 EUDAMEDFDA UDI
Basic UDI-DI
0693856IOSGU EUDAMED
++D090ClassIJE EUDAMED
FDA Product Code
NOF FDA UDI
EMDN Code
Z12110101 DENTAL TREATMENT UNITS EUDAMED
V9099 VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - OTHER EUDAMED
GMDN Term
Intraoral optical scanning system FDA UDI

Classification

Device Class
Class I EUDAMED
Class II FDA UDI
Regulation Number
872.3661 FDA UDI
Market of Registration
Finland EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Dental delivery system

IS 3600 I/O 3D Scanner by Dental Imaging Technologies Corporation — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental delivery system.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
US-MF-000017139
Authorised Representative
PaloDEx Group Oy FI-AR-000004955

Sources (3)

  • EUDAMED 014ec6b9-9ddc-420d-8cc1-773916183e3c 61 fields · synced Oct 6, 2026
  • FDA UDI 96905da4-17cb-4fc0-9b60-d1a64768efef 33 fields · synced May 30, 2026
  • EUDAMED 23b3edf6-0105-44b5-82e7-13a3ec4aeef3 61 fields · synced Jul 12, 2026