gudid
Primary ID: 836 018
N/A (UDI 836 018)
Manufactured by MEDTRONIC SOFAMOR DANEK, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for N/A - Primary ID 836 018
Device Regulatory Overview
The N/A (Model/Catalog Number: 836 018) is a medical device manufactured by MEDTRONIC SOFAMOR DANEK, INC.. This product is indexed under FDA Product Code / Category Classification DZP within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 836 018
- Product Code / EMDN
- DZP
- Device Name
- INSTRUMENT 836-018 SOLID TAP 7.5MM
- Database Sync Date
- 2026-08-09 09:07:45
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 N/A?
The registered manufacturer of record for N/A is MEDTRONIC SOFAMOR DANEK, INC..
What is the Primary UDI-DI identifier for N/A?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 836 018.
What classification code is assigned to this device?
This device is registered under product classification code DZP.
Similar Classification Devices (DZP)
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint