Subtilis Wundhaken Roux Fig.1, 16,5 cm, 20 x 22 mm, 25 x 26 mm (UDI 07640229295424)
Manufactured by Accuratus AG
Device Regulatory Overview
The Subtilis Wundhaken Roux Fig.1, 16,5 cm, 20 x 22 mm, 25 x 26 mm (Model/Catalog Number: 24.06.04) is a medical device manufactured by Accuratus AG. This product is indexed under FDA Product Code / Category Classification L0902 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 24.06.04
- Product Code / EMDN
- L0902
- Device Name
- Subtilis Wundhaken Roux Fig.1, 16,5 cm, 20 x 22 mm, 25 x 26 mm
- Database Sync Date
- 2026-08-09 16:29:03
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 Subtilis Wundhaken Roux Fig.1, 16,5 cm, 20 x 22 mm, 25 x 26 mm?
The registered manufacturer of record for Subtilis Wundhaken Roux Fig.1, 16,5 cm, 20 x 22 mm, 25 x 26 mm is Accuratus AG.
What is the Primary UDI-DI identifier for Subtilis Wundhaken Roux Fig.1, 16,5 cm, 20 x 22 mm, 25 x 26 mm?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 07640229295424.
What classification code is assigned to this device?
This device is registered under product classification code L0902.
Similar Classification Devices (L0902)
Other Devices by Accuratus AG
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint