BMV® Foam-Trachealkompresse 969 oval, Standard (UDI 04251242695257)
Manufactured by BMV Bender Medical Vertrieb GmbH
Device Regulatory Overview
The BMV® Foam-Trachealkompresse 969 oval, Standard (Model/Catalog Number: 116011) is a medical device manufactured by BMV Bender Medical Vertrieb GmbH. This product is indexed under FDA Product Code / Category Classification R01058099 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 116011
- Product Code / EMDN
- R01058099
- Device Name
- Trachealkompresse
- Database Sync Date
- 2026-08-09 16:28:46
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 BMV® Foam-Trachealkompresse 969 oval, Standard?
The registered manufacturer of record for BMV® Foam-Trachealkompresse 969 oval, Standard is BMV Bender Medical Vertrieb GmbH.
What is the Primary UDI-DI identifier for BMV® Foam-Trachealkompresse 969 oval, Standard?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04251242695257.
What classification code is assigned to this device?
This device is registered under product classification code R01058099.
Similar Classification Devices (R01058099)
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