gudid
Primary ID: 3350
ClearLook CeraSpoon (UDI 3350)
Manufactured by Bionix, LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ClearLook CeraSpoon - Primary ID 3350
Device Regulatory Overview
The ClearLook CeraSpoon (Model/Catalog Number: 3350) is a medical device manufactured by Bionix, LLC. This product is indexed under FDA Product Code / Category Classification JYG within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 3350
- Product Code / EMDN
- JYG
- Device Name
- ClearLook CeraSpoon
- Database Sync Date
- 2026-08-09 09:04:11
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 ClearLook CeraSpoon?
The registered manufacturer of record for ClearLook CeraSpoon is Bionix, LLC.
What is the Primary UDI-DI identifier for ClearLook CeraSpoon?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 3350.
What classification code is assigned to this device?
This device is registered under product classification code JYG.
Similar Classification Devices (JYG)
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint