gudid
Primary ID: N/A
Auto-Prep Unit for AIA-CL1200 (UDI N/A)
Manufactured by TOSOH CORPORATION
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Auto-Prep Unit for AIA-CL1200 - Primary ID N/A
Device Regulatory Overview
The Auto-Prep Unit for AIA-CL1200 (Model/Catalog Number: N/A) is a medical device manufactured by TOSOH CORPORATION. This product is indexed under FDA Product Code / Category Classification JJE within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- N/A
- Product Code / EMDN
- JJE
- Device Name
- Database Sync Date
- 2026-08-09 09:15:39
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 Auto-Prep Unit for AIA-CL1200?
The registered manufacturer of record for Auto-Prep Unit for AIA-CL1200 is TOSOH CORPORATION.
What is the Primary UDI-DI identifier for Auto-Prep Unit for AIA-CL1200?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is N/A.
What classification code is assigned to this device?
This device is registered under product classification code JJE.
Similar Classification Devices (JJE)
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