← Back to catalogue

ORTHOPANTOMOGRAPH™ OP 3D Pro

EUDAMEDFDA UDI

Class IIb (EU MDR)

Ref 901005Model OP300-1

by PaloDEx Group Oy

Identity

Trade Name
ORTHOPANTOMOGRAPH™ OP 3D Pro EUDAMED
ORTHOPANTOMOGRAPH OP 3D Pro FDA UDI
Generic Name
Limited-view-field CT system FDA UDI
Device Name
ORTHOPANTOMOGRAPH™ OP 3D Pro EUDAMED
Model / Reference
OP300-1 EUDAMEDFDA UDI
901005 EUDAMED

Identifiers

Catalog Number
901005 FDA UDI
Primary DI / UDI-DI
06430035872763 EUDAMEDFDA UDI
Basic UDI-DI
B-06430035872763 EUDAMED
510(k) Number
K133544 FDA UDI
FDA Product Code
OAS FDA UDI
EMDN Code
Z11030507 TOMOGRAPHS EUDAMED
GMDN Term
Limited-view-field CT system FDA UDI

Classification

Device Class
Class IIb EUDAMED
Class II FDA UDI
Regulation Number
892.1750 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

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Prescription Use

Yes

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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

ORTHOPANTOMOGRAPH™ OP 3D Pro by PaloDEx Group Oy — Class IIb — MDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDD

United States Pending data

FDA UDI

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

Manufacturer

Manufacturer
PaloDEx Group Oy
EUDAMED SRN
FI-MF-000004943

Sources (2)

  • EUDAMED eb60d1f4-04dd-4bb8-897a-330f49a8a44e 61 fields · synced Jun 19, 2026
  • FDA UDI 0828e592-e764-4283-baf2-a144b237280f 35 fields · synced May 30, 2026