gudid
Primary ID: 70001
Apex (UDI 70001)
Manufactured by Drive Devilbiss Healthcare
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Apex - Primary ID 70001
Device Regulatory Overview
The Apex (Model/Catalog Number: 70001) is a medical device manufactured by Drive Devilbiss Healthcare. This product is indexed under FDA Product Code / Category Classification KYX within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 70001
- Product Code / EMDN
- KYX
- Device Name
- MEDICINE SPOON
- Database Sync Date
- 2026-08-09 09:08:46
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 Apex?
The registered manufacturer of record for Apex is Drive Devilbiss Healthcare.
What is the Primary UDI-DI identifier for Apex?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 70001.
What classification code is assigned to this device?
This device is registered under product classification code KYX.
Similar Classification Devices (KYX)
Other Devices by Drive Devilbiss Healthcare
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint