eudamed_udi
Primary ID: 06430035872879
ORTHOPANTOMOGRAPH™ OP 3D (UDI 06430035872879)
Manufactured by PaloDEx Group Oy
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ORTHOPANTOMOGRAPH™ OP 3D - Primary ID 06430035872879
Device Regulatory Overview
The ORTHOPANTOMOGRAPH™ OP 3D (Model/Catalog Number: 900989) is a medical device manufactured by PaloDEx Group Oy. This product is indexed under FDA Product Code / Category Classification Z11030507 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 900989
- Product Code / EMDN
- Z11030507
- Device Name
- ORTHOPANTOMOGRAPH™ OP 3D
- Database Sync Date
- 2026-08-09 16:44:59
Full Regulatory Attributes
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{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of ORTHOPANTOMOGRAPH™ OP 3D?
The registered manufacturer of record for ORTHOPANTOMOGRAPH™ OP 3D is PaloDEx Group Oy.
What is the Primary UDI-DI identifier for ORTHOPANTOMOGRAPH™ OP 3D?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06430035872879.
What classification code is assigned to this device?
This device is registered under product classification code Z11030507.
Similar Classification Devices (Z11030507)
Other Devices by PaloDEx Group Oy
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