gudid
Primary ID: 2730
n/a (UDI 2730)
Manufactured by HANS RUDOLPH, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for n/a - Primary ID 2730
Device Regulatory Overview
The n/a (Model/Catalog Number: 2730) is a medical device manufactured by HANS RUDOLPH, INC.. This product is indexed under FDA Product Code / Category Classification EJL within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 2730
- Product Code / EMDN
- EJL
- Device Name
- 2730 2WAY NRBV LG Y SHAPE
- Database Sync Date
- 2026-08-09 09:07:42
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 n/a?
The registered manufacturer of record for n/a is HANS RUDOLPH, INC..
What is the Primary UDI-DI identifier for n/a?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 2730.
What classification code is assigned to this device?
This device is registered under product classification code EJL.
Similar Classification Devices (EJL)
Other Devices by HANS RUDOLPH, INC.
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