A-Raspel VEKTOR-Titan Vierkantanschluss 8/10 (UDI 04029839613645)
Manufactured by Peter Brehm GmbH
Device Regulatory Overview
The A-Raspel VEKTOR-Titan Vierkantanschluss 8/10 (Model/Catalog Number: 61402-15) is a medical device manufactured by Peter Brehm GmbH. This product is indexed under FDA Product Code / Category Classification L091199 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 61402-15
- Product Code / EMDN
- L091199
- Device Name
- A-Raspel VEKTOR-Titan Vierkantanschluss 8/10
- Database Sync Date
- 2026-08-09 16:29:22
Full Regulatory Attributes
đź”’ Token Gated
{
"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 A-Raspel VEKTOR-Titan Vierkantanschluss 8/10?
The registered manufacturer of record for A-Raspel VEKTOR-Titan Vierkantanschluss 8/10 is Peter Brehm GmbH.
What is the Primary UDI-DI identifier for A-Raspel VEKTOR-Titan Vierkantanschluss 8/10?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04029839613645.
What classification code is assigned to this device?
This device is registered under product classification code L091199.
Similar Classification Devices (L091199)
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