Wewa® Med Rückenstützorthese für Damen mit Zwickel (UDI 04048486069810)
Manufactured by Werkmeister GmbH + Co. KG
Device Regulatory Overview
The Wewa® Med Rückenstützorthese für Damen mit Zwickel (Model/Catalog Number: S/3334) is a medical device manufactured by Werkmeister GmbH + Co. KG. This product is indexed under FDA Product Code / Category Classification Y060309 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- S/3334
- Product Code / EMDN
- Y060309
- Device Name
- Rumpfstützorthese
- Database Sync Date
- 2026-08-09 16:29:05
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 Wewa® Med Rückenstützorthese für Damen mit Zwickel?
The registered manufacturer of record for Wewa® Med Rückenstützorthese für Damen mit Zwickel is Werkmeister GmbH + Co. KG.
What is the Primary UDI-DI identifier for Wewa® Med Rückenstützorthese für Damen mit Zwickel?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04048486069810.
What classification code is assigned to this device?
This device is registered under product classification code Y060309.
Similar Classification Devices (Y060309)
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint