Verschlusskappen für purVENT für Bajonettverschluss** (UDI 04260741290290)
Manufactured by Theodor Labarre Werkstätte für silb. chirurg. Instrumente GmbH
Device Regulatory Overview
The Verschlusskappen für purVENT für Bajonettverschluss** (Model/Catalog Number: 10682) is a medical device manufactured by Theodor Labarre Werkstätte für silb. chirurg. Instrumente GmbH. This product is indexed under FDA Product Code / Category Classification R01058099 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 10682
- Product Code / EMDN
- R01058099
- Device Name
- Verschlusskappen
- Database Sync Date
- 2026-08-09 16:30:07
Full Regulatory Attributes
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{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Verschlusskappen für purVENT für Bajonettverschluss**?
The registered manufacturer of record for Verschlusskappen für purVENT für Bajonettverschluss** is Theodor Labarre Werkstätte für silb. chirurg. Instrumente GmbH.
What is the Primary UDI-DI identifier for Verschlusskappen für purVENT für Bajonettverschluss**?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04260741290290.
What classification code is assigned to this device?
This device is registered under product classification code R01058099.
Similar Classification Devices (R01058099)
Other Devices by Theodor Labarre Werkstätte für silb. chirurg. Instrumente GmbH
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