eudamed_udi
Primary ID: 08023279267754
SPECULUM NASALE VOLTOLINI Nr. 0 - regolabile (UDI 08023279267754)
Manufactured by GIMA SPA
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for SPECULUM NASALE VOLTOLINI Nr. 0 - regolabile - Primary ID 08023279267754
Device Regulatory Overview
The SPECULUM NASALE VOLTOLINI Nr. 0 - regolabile (Model/Catalog Number: 26775) is a medical device manufactured by GIMA SPA. This product is indexed under FDA Product Code / Category Classification L149004 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 26775
- Product Code / EMDN
- L149004
- Device Name
- SPECULUM ORL RIUTILIZZABILI
- Database Sync Date
- 2026-08-09 16:29:36
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 SPECULUM NASALE VOLTOLINI Nr. 0 - regolabile?
The registered manufacturer of record for SPECULUM NASALE VOLTOLINI Nr. 0 - regolabile is GIMA SPA.
What is the Primary UDI-DI identifier for SPECULUM NASALE VOLTOLINI Nr. 0 - regolabile?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08023279267754.
What classification code is assigned to this device?
This device is registered under product classification code L149004.
Similar Classification Devices (L149004)
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