DUNITECH (UDI 08681124119810)
Manufactured by Oliga Makina Elektronik İthalat İhracat Sanayi ve Ticaret Limited Şirketi
Device Regulatory Overview
The DUNITECH (Model/Catalog Number: NEON-155-000) is a medical device manufactured by Oliga Makina Elektronik İthalat İhracat Sanayi ve Ticaret Limited Şirketi. This product is indexed under FDA Product Code / Category Classification P09120604 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- NEON-155-000
- Product Code / EMDN
- P09120604
- Device Name
- PROXIMAL END CAP 00mm (FLUSH) (Ti)
- Database Sync Date
- 2026-08-09 16:29:47
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of DUNITECH?
The registered manufacturer of record for DUNITECH is Oliga Makina Elektronik İthalat İhracat Sanayi ve Ticaret Limited Şirketi.
What is the Primary UDI-DI identifier for DUNITECH?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08681124119810.
What classification code is assigned to this device?
This device is registered under product classification code P09120604.
Similar Classification Devices (P09120604)
Other Devices by Oliga Makina Elektronik İthalat İhracat Sanayi ve Ticaret Limited Şirketi
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint