Evolution+ Body Fluid Disposal (UDI 05037331018393)
Manufactured by Safety First Aid Group Limited
Device Regulatory Overview
The Evolution+ Body Fluid Disposal (Model/Catalog Number: K395EV) is a medical device manufactured by Safety First Aid Group Limited. This product is indexed under FDA Product Code / Category Classification V0501 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- K395EV
- Product Code / EMDN
- V0501
- Device Name
- First Aid Kits
- Database Sync Date
- 2026-08-09 16:46:03
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 Evolution+ Body Fluid Disposal?
The registered manufacturer of record for Evolution+ Body Fluid Disposal is Safety First Aid Group Limited.
What is the Primary UDI-DI identifier for Evolution+ Body Fluid Disposal?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05037331018393.
What classification code is assigned to this device?
This device is registered under product classification code V0501.
Similar Classification Devices (V0501)
Other Devices by Safety First Aid Group Limited
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint