Alexis Wound Protector-Retractor (UDI 00607915132958)
Manufactured by Applied Medical Resources Corporation
Device Regulatory Overview
The Alexis Wound Protector-Retractor (Model/Catalog Number: C8322) is a medical device manufactured by Applied Medical Resources Corporation. This product is indexed under FDA Product Code / Category Classification K01020106 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- C8322
- Product Code / EMDN
- K01020106
- Device Name
- Alexisยฎ (O) Wound Protector-Retractors
- Database Sync Date
- 2026-08-09 16:28:50
Full Regulatory Attributes
๐ 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 Alexis Wound Protector-Retractor?
The registered manufacturer of record for Alexis Wound Protector-Retractor is Applied Medical Resources Corporation.
What is the Primary UDI-DI identifier for Alexis Wound Protector-Retractor?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00607915132958.
What classification code is assigned to this device?
This device is registered under product classification code K01020106.
Similar Classification Devices (K01020106)
Other Devices by Applied Medical Resources Corporation
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint