eudamed_udi
Primary ID: 08054529351626
NOVOX DROP 5mL - 1 pc. (UDI 08054529351626)
Manufactured by MOSS S.p.A.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for NOVOX DROP 5mL - 1 pc. - Primary ID 08054529351626
Device Regulatory Overview
The NOVOX DROP 5mL - 1 pc. (Model/Catalog Number: NDS005S-L2) is a medical device manufactured by MOSS S.p.A.. This product is indexed under FDA Product Code / Category Classification M040413 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- NDS005S-L2
- Product Code / EMDN
- M040413
- Device Name
- NOVOX DROP
- Database Sync Date
- 2026-08-09 16:59:36
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 NOVOX DROP 5mL - 1 pc.?
The registered manufacturer of record for NOVOX DROP 5mL - 1 pc. is MOSS S.p.A..
What is the Primary UDI-DI identifier for NOVOX DROP 5mL - 1 pc.?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08054529351626.
What classification code is assigned to this device?
This device is registered under product classification code M040413.
Similar Classification Devices (M040413)
Other Devices by MOSS S.p.A.
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