eudamed_udi
Primary ID: 10812594012577
NeoSucker® Curved Extra Large (UDI 10812594012577)
Manufactured by Neotech Products LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for NeoSucker® Curved Extra Large - Primary ID 10812594012577
Device Regulatory Overview
The NeoSucker® Curved Extra Large (Model/Catalog Number: N208) is a medical device manufactured by Neotech Products LLC. This product is indexed under FDA Product Code / Category Classification R05010301 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- N208
- Product Code / EMDN
- R05010301
- Device Name
- Little Sucker®
- Database Sync Date
- 2026-08-09 17:02:47
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 NeoSucker® Curved Extra Large?
The registered manufacturer of record for NeoSucker® Curved Extra Large is Neotech Products LLC.
What is the Primary UDI-DI identifier for NeoSucker® Curved Extra Large?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 10812594012577.
What classification code is assigned to this device?
This device is registered under product classification code R05010301.
Similar Classification Devices (R05010301)
Other Devices by Neotech Products LLC
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