gudid
Primary ID: 20g powder
Endoseal (UDI 20g powder)
Manufactured by PREVEST DENPRO LIMITED
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Endoseal - Primary ID 20g powder
Device Regulatory Overview
The Endoseal (Model/Catalog Number: 20g powder) is a medical device manufactured by PREVEST DENPRO LIMITED. This product is indexed under FDA Product Code / Category Classification KIF within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 20g powder
- Product Code / EMDN
- KIF
- Device Name
- Database Sync Date
- 2026-08-09 09:01:11
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 Endoseal?
The registered manufacturer of record for Endoseal is PREVEST DENPRO LIMITED.
What is the Primary UDI-DI identifier for Endoseal?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 20g powder.
What classification code is assigned to this device?
This device is registered under product classification code KIF.
Similar Classification Devices (KIF)
Other Devices by PREVEST DENPRO LIMITED
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint