eudamed_udi
Primary ID: 08964004689338
EAR LEVER BUTTONED ACCORDING TO LUCAE MEDIUM (UDI 08964004689338)
Manufactured by Ayyat Steel
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for EAR LEVER BUTTONED ACCORDING TO LUCAE MEDIUM - Primary ID 08964004689338
Device Regulatory Overview
The EAR LEVER BUTTONED ACCORDING TO LUCAE MEDIUM (Model/Catalog Number: 20-6001.01) is a medical device manufactured by Ayyat Steel. This product is indexed under FDA Product Code / Category Classification K01020112 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 20-6001.01
- Product Code / EMDN
- K01020112
- Device Name
- EAR LEVER BUTTONED ACCORDING TO LUCAE MEDIUM
- Database Sync Date
- 2026-08-09 18:57:26
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 EAR LEVER BUTTONED ACCORDING TO LUCAE MEDIUM?
The registered manufacturer of record for EAR LEVER BUTTONED ACCORDING TO LUCAE MEDIUM is Ayyat Steel.
What is the Primary UDI-DI identifier for EAR LEVER BUTTONED ACCORDING TO LUCAE MEDIUM?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08964004689338.
What classification code is assigned to this device?
This device is registered under product classification code K01020112.
Similar Classification Devices (K01020112)
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint