gudid
Primary ID: 0702020001
Neptune 2 (UDI 0702020001)
Manufactured by STRYKER CORPORATION
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Neptune 2 - Primary ID 0702020001
Device Regulatory Overview
The Neptune 2 (Model/Catalog Number: 0702020001) is a medical device manufactured by STRYKER CORPORATION. This product is indexed under FDA Product Code / Category Classification JCX within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 0702020001
- Product Code / EMDN
- JCX
- Device Name
- Specimen Collection 4-Port Manifold
- Database Sync Date
- 2026-08-09 09:45:30
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 2?
The registered manufacturer of record for Neptune 2 is STRYKER CORPORATION.
What is the Primary UDI-DI identifier for Neptune 2?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 0702020001.
What classification code is assigned to this device?
This device is registered under product classification code JCX.
Similar Classification Devices (JCX)
Other Devices by STRYKER CORPORATION
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