N/A (UDI 836 010)
Manufactured by Smith & Nephew, Inc.
Device Regulatory Overview
The N/A (Model/Catalog Number: 836 010) is a medical device manufactured by Smith & Nephew, Inc.. This product is indexed under FDA Product Code / Category Classification DZP within international Unique Device Identification (UDI) compliance databases.
Enforcement actions are currently active for this product line.
TRIGEN PROXIMAL STRAIGHT HUMERAL NAIL 8/7 X 16, REF: 71760816...
BIOSURE HA SCREW, 6MM x 20 MM. Threaded metallic bone fixation fastener....
META-TAN LAG/COMPRESSION SCREW KIT 90MM/85MM, REF: 71642690...
Technical Specifications
- Model Number
- 836 010
- Product Code / EMDN
- DZP
- Device Name
- GRSPR D/A ATRAUMATIC 5MMX36CM
- 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 Smith & Nephew, Inc..
What is the Primary UDI-DI identifier for N/A?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 836 010.
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