gudid
Primary ID: 1487000
AggRAM Module (110/220 V) (UDI 1487000)
Manufactured by HELENA LABORATORIES CORPORATION
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for AggRAM Module (110/220 V) - Primary ID 1487000
Device Regulatory Overview
The AggRAM Module (110/220 V) (Model/Catalog Number: 1487000) is a medical device manufactured by HELENA LABORATORIES CORPORATION. This product is indexed under FDA Product Code / Category Classification JPA within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 1487000
- Product Code / EMDN
- JPA
- Device Name
- Database Sync Date
- 2026-08-09 09:36:16
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 AggRAM Module (110/220 V)?
The registered manufacturer of record for AggRAM Module (110/220 V) is HELENA LABORATORIES CORPORATION.
What is the Primary UDI-DI identifier for AggRAM Module (110/220 V)?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 1487000.
What classification code is assigned to this device?
This device is registered under product classification code JPA.
Similar Classification Devices (JPA)
Other Devices by HELENA LABORATORIES CORPORATION
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