gudid
Primary ID: 1030
N/A (UDI 1030)
Manufactured by GALEMED CORPORATION
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for N/A - Primary ID 1030
Device Regulatory Overview
The N/A (Model/Catalog Number: 1030) is a medical device manufactured by GALEMED CORPORATION. This product is indexed under FDA Product Code / Category Classification BYE within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 1030
- Product Code / EMDN
- BYE
- Device Name
- 12.5 cmH2O Pressure Relief Manifold
- Database Sync Date
- 2026-08-09 09:15:32
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 N/A?
The registered manufacturer of record for N/A is GALEMED CORPORATION.
What is the Primary UDI-DI identifier for N/A?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 1030.
What classification code is assigned to this device?
This device is registered under product classification code BYE.
Similar Classification Devices (BYE)
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