gudid
Primary ID: 5026161U0
Brasseler USA (UDI 5026161U0)
Manufactured by Peter Brasseler Holdings, LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Brasseler USA - Primary ID 5026161U0
Device Regulatory Overview
The Brasseler USA (Model/Catalog Number: 5026161U0) is a medical device manufactured by Peter Brasseler Holdings, LLC. This product is indexed under FDA Product Code / Category Classification EIK within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 5026161U0
- Product Code / EMDN
- EIK
- Device Name
- PKT3R6 PKT 3 ROUND END #6 HDL
- Database Sync Date
- 2026-08-09 09:24:26
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 Brasseler USA?
The registered manufacturer of record for Brasseler USA is Peter Brasseler Holdings, LLC.
What is the Primary UDI-DI identifier for Brasseler USA?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 5026161U0.
What classification code is assigned to this device?
This device is registered under product classification code EIK.
Similar Classification Devices (EIK)
Other Devices by Peter Brasseler Holdings, LLC
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