gudid
Primary ID: 6151A2
Renamel Microfill (UDI 6151A2)
Manufactured by DeltaMed GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Renamel Microfill - Primary ID 6151A2
Device Regulatory Overview
The Renamel Microfill (Model/Catalog Number: 6151A2) is a medical device manufactured by DeltaMed GmbH. This product is indexed under FDA Product Code / Category Classification EBF within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 6151A2
- Product Code / EMDN
- EBF
- Device Name
- Renamel Microfill Enamel Body A2, Syringe 2g
- 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 Microfill?
The registered manufacturer of record for Renamel Microfill is DeltaMed GmbH.
What is the Primary UDI-DI identifier for Renamel Microfill?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 6151A2.
What classification code is assigned to this device?
This device is registered under product classification code EBF.
Similar Classification Devices (EBF)
Other Devices by DeltaMed GmbH
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