gudid
Primary ID: 6161A1
Renamel Microhybrid (UDI 6161A1)
Manufactured by DeltaMed GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Renamel Microhybrid - Primary ID 6161A1
Device Regulatory Overview
The Renamel Microhybrid (Model/Catalog Number: 6161A1) 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
- 6161A1
- Product Code / EMDN
- EBF
- Device Name
- Renamel Microhybrid Body A1, 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 Microhybrid?
The registered manufacturer of record for Renamel Microhybrid is DeltaMed GmbH.
What is the Primary UDI-DI identifier for Renamel Microhybrid?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 6161A1.
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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