eudamed_udi
Primary ID: 08053178791920
CIOTOLA BLU DA 3000 ML CON GUIDE (UDI 08053178791920)
Manufactured by Surgika srl
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for CIOTOLA BLU DA 3000 ML CON GUIDE - Primary ID 08053178791920
Device Regulatory Overview
The CIOTOLA BLU DA 3000 ML CON GUIDE (Model/Catalog Number: C06ALL0407) is a medical device manufactured by Surgika srl. This product is indexed under FDA Product Code / Category Classification T0306 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- C06ALL0407
- Product Code / EMDN
- T0306
- Device Name
- Protezioni per pazienti durante procedure cliniche-Protections for patients under clinical procedures
- Database Sync Date
- 2026-08-09 16:47:14
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 CIOTOLA BLU DA 3000 ML CON GUIDE?
The registered manufacturer of record for CIOTOLA BLU DA 3000 ML CON GUIDE is Surgika srl.
What is the Primary UDI-DI identifier for CIOTOLA BLU DA 3000 ML CON GUIDE?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08053178791920.
What classification code is assigned to this device?
This device is registered under product classification code T0306.
Similar Classification Devices (T0306)
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