eudamed_udi
Primary ID: 08806182202834
Wound Retractor (UDI 08806182202834)
Manufactured by SEJONG MEDICAL Co., Ltd.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Wound Retractor - Primary ID 08806182202834
Device Regulatory Overview
The Wound Retractor (Model/Catalog Number: WR-12-195) is a medical device manufactured by SEJONG MEDICAL Co., Ltd.. This product is indexed under FDA Product Code / Category Classification K01020106 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- WR-12-195
- Product Code / EMDN
- K01020106
- Device Name
- Wound Retractor
- Database Sync Date
- 2026-08-09 16:29:11
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 Wound Retractor?
The registered manufacturer of record for Wound Retractor is SEJONG MEDICAL Co., Ltd..
What is the Primary UDI-DI identifier for Wound Retractor?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08806182202834.
What classification code is assigned to this device?
This device is registered under product classification code K01020106.
Similar Classification Devices (K01020106)
Other Devices by SEJONG MEDICAL Co., Ltd.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint