eudamed_udi
Primary ID: 05425023685082
Neptune Instrument (UDI 05425023685082)
Manufactured by D-tek s.a.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Neptune Instrument - Primary ID 05425023685082
Device Regulatory Overview
The Neptune Instrument (Model/Catalog Number: DIA1000) is a medical device manufactured by D-tek s.a.. This product is indexed under FDA Product Code / Category Classification W0201020101 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- DIA1000
- Product Code / EMDN
- W0201020101
- Device Name
- BlueDiver Instrument I
- Database Sync Date
- 2026-08-09 16:51:45
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 Neptune Instrument?
The registered manufacturer of record for Neptune Instrument is D-tek s.a..
What is the Primary UDI-DI identifier for Neptune Instrument?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05425023685082.
What classification code is assigned to this device?
This device is registered under product classification code W0201020101.
Similar Classification Devices (W0201020101)
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