gudid
Primary ID: 9015
9015 REUSABLE NOSECLIPS (UDI 9015)
Manufactured by HANS RUDOLPH, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for 9015 REUSABLE NOSECLIPS - Primary ID 9015
Device Regulatory Overview
The 9015 REUSABLE NOSECLIPS (Model/Catalog Number: 9015) is a medical device manufactured by HANS RUDOLPH, INC.. This product is indexed under FDA Product Code / Category Classification BXJ within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 9015
- Product Code / EMDN
- BXJ
- Device Name
- NOSE CLIP ASSY REUSEABLE 9015
- 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 9015 REUSABLE NOSECLIPS?
The registered manufacturer of record for 9015 REUSABLE NOSECLIPS is HANS RUDOLPH, INC..
What is the Primary UDI-DI identifier for 9015 REUSABLE NOSECLIPS?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 9015.
What classification code is assigned to this device?
This device is registered under product classification code BXJ.
Similar Classification Devices (BXJ)
Other Devices by HANS RUDOLPH, INC.
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