eudamed_udi
Primary ID: 18051380470005
Bacinella reniforme (UDI 18051380470005)
Manufactured by CARBON NEMO SRL
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Bacinella reniforme - Primary ID 18051380470005
Device Regulatory Overview
The Bacinella reniforme (Model/Catalog Number: 0076) is a medical device manufactured by CARBON NEMO SRL. This product is indexed under FDA Product Code / Category Classification V0402 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 0076
- Product Code / EMDN
- V0402
- Device Name
- BACINELLA RENIFORME IN PET MONOUSO
- Database Sync Date
- 2026-08-09 16:47:05
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 Bacinella reniforme?
The registered manufacturer of record for Bacinella reniforme is CARBON NEMO SRL.
What is the Primary UDI-DI identifier for Bacinella reniforme?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 18051380470005.
What classification code is assigned to this device?
This device is registered under product classification code V0402.
Similar Classification Devices (V0402)
Other Devices by CARBON NEMO SRL
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