gudid
Primary ID: 5530
5530 7L SYRINGE (UDI 5530)
Manufactured by HANS RUDOLPH, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for 5530 7L SYRINGE - Primary ID 5530
Device Regulatory Overview
The 5530 7L SYRINGE (Model/Catalog Number: 5530) is a medical device manufactured by HANS RUDOLPH, INC.. This product is indexed under FDA Product Code / Category Classification BXW within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 5530
- Product Code / EMDN
- BXW
- Device Name
- 5530 SYR W/SMC ID TPR FM OUTLT
- Database Sync Date
- 2026-08-09 09:31:22
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 5530 7L SYRINGE?
The registered manufacturer of record for 5530 7L SYRINGE is HANS RUDOLPH, INC..
What is the Primary UDI-DI identifier for 5530 7L SYRINGE?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 5530.
What classification code is assigned to this device?
This device is registered under product classification code BXW.
Similar Classification Devices (BXW)
Other Devices by HANS RUDOLPH, INC.
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