gudid
Primary ID: 7011C4
Renamel Flowable Microhybrid (UDI 7011C4)
Manufactured by DeltaMed GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Renamel Flowable Microhybrid - Primary ID 7011C4
Device Regulatory Overview
The Renamel Flowable Microhybrid (Model/Catalog Number: 7011C4) is a medical device manufactured by DeltaMed GmbH. This product is indexed under FDA Product Code / Category Classification EBD within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 7011C4
- Product Code / EMDN
- EBD
- Device Name
- Renamel Flowable Microhybrid Body C4, Syringe 3g
- Database Sync Date
- 2026-08-09 09:05:54
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 Renamel Flowable Microhybrid?
The registered manufacturer of record for Renamel Flowable Microhybrid is DeltaMed GmbH.
What is the Primary UDI-DI identifier for Renamel Flowable Microhybrid?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 7011C4.
What classification code is assigned to this device?
This device is registered under product classification code EBD.
Similar Classification Devices (EBD)
Other Devices by DeltaMed GmbH
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