eudamed_udi
Primary ID: 00724995356248
RAPIDAER Hookup (UDI 00724995356248)
Manufactured by STERIS Italy S.r.l.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for RAPIDAER Hookup - Primary ID 00724995356248
Device Regulatory Overview
The RAPIDAER Hookup (Model/Catalog Number: LARAH318) is a medical device manufactured by STERIS Italy S.r.l.. This product is indexed under FDA Product Code / Category Classification Z12011399 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- LARAH318
- Product Code / EMDN
- Z12011399
- Device Name
- RAPIDAER Endoscope Reprocessor Hookups
- Database Sync Date
- 2026-08-09 16:29:36
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 RAPIDAER Hookup?
The registered manufacturer of record for RAPIDAER Hookup is STERIS Italy S.r.l..
What is the Primary UDI-DI identifier for RAPIDAER Hookup?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00724995356248.
What classification code is assigned to this device?
This device is registered under product classification code Z12011399.
Similar Classification Devices (Z12011399)
Other Devices by STERIS Italy S.r.l.
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