gudid
Primary ID: 10-100
Brasseler USA (UDI 10-100)
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 10-100
Device Regulatory Overview
The Brasseler USA (Model/Catalog Number: 10-100) is a medical device manufactured by Peter Brasseler Holdings, LLC. This product is indexed under FDA Product Code / Category Classification HSZ within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 10-100
- Product Code / EMDN
- HSZ
- Device Name
- 10-100 Versadriver Pneumatic
- 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 10-100.
What classification code is assigned to this device?
This device is registered under product classification code HSZ.
Similar Classification Devices (HSZ)
Other Devices by Peter Brasseler Holdings, LLC
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