ROSEN Ohrtrichter 6 mm geschlitzt schwarz (UDI 04250485306135)
Manufactured by Zepf Medical Instruments GmbH
Device Regulatory Overview
The ROSEN Ohrtrichter 6 mm geschlitzt schwarz (Model/Catalog Number: 99-9016-61) is a medical device manufactured by Zepf Medical Instruments GmbH. This product is indexed under FDA Product Code / Category Classification L149004 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 99-9016-61
- Product Code / EMDN
- L149004
- Device Name
- Spekulum, Ohr
- Database Sync Date
- 2026-08-09 16:29:58
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 ROSEN Ohrtrichter 6 mm geschlitzt schwarz?
The registered manufacturer of record for ROSEN Ohrtrichter 6 mm geschlitzt schwarz is Zepf Medical Instruments GmbH.
What is the Primary UDI-DI identifier for ROSEN Ohrtrichter 6 mm geschlitzt schwarz?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04250485306135.
What classification code is assigned to this device?
This device is registered under product classification code L149004.
Similar Classification Devices (L149004)
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint