gudid
Primary ID: A9513
PT,STORAGE MODULE,LAM TOP,32hx24wx42d (UDI A9513)
Manufactured by Hausmann Enterprises, LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for PT,STORAGE MODULE,LAM TOP,32hx24wx42d - Primary ID A9513
Device Regulatory Overview
The PT,STORAGE MODULE,LAM TOP,32hx24wx42d (Model/Catalog Number: A9513) is a medical device manufactured by Hausmann Enterprises, LLC. This product is indexed under FDA Product Code / Category Classification KMN within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- A9513
- Product Code / EMDN
- KMN
- Device Name
- Database Sync Date
- 2026-08-09 09:23:12
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 PT,STORAGE MODULE,LAM TOP,32hx24wx42d?
The registered manufacturer of record for PT,STORAGE MODULE,LAM TOP,32hx24wx42d is Hausmann Enterprises, LLC.
What is the Primary UDI-DI identifier for PT,STORAGE MODULE,LAM TOP,32hx24wx42d?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is A9513.
What classification code is assigned to this device?
This device is registered under product classification code KMN.
Similar Classification Devices (KMN)
Other Devices by Hausmann Enterprises, LLC
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