gudid
Primary ID: Assorted - Suction
NeoHug (UDI Assorted - Suction)
Manufactured by Neotech Products LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for NeoHug - Primary ID Assorted - Suction
Device Regulatory Overview
The NeoHug (Model/Catalog Number: Assorted - Suction) is a medical device manufactured by Neotech Products LLC. This product is indexed under FDA Product Code / Category Classification JAY within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- Assorted - Suction
- Product Code / EMDN
- JAY
- Device Name
- NeoHug is intended to support, organize or hold non-operating medical devices.
- Database Sync Date
- 2026-08-09 09:43:40
Full Regulatory Attributes
🔒 Token Gated
{
"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 NeoHug?
The registered manufacturer of record for NeoHug is Neotech Products LLC.
What is the Primary UDI-DI identifier for NeoHug?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is Assorted - Suction.
What classification code is assigned to this device?
This device is registered under product classification code JAY.
Similar Classification Devices (JAY)
Other Devices by Neotech Products LLC
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