gudid
Primary ID: INVALID PRODUCT
ManaMed Inc (UDI INVALID PRODUCT)
Manufactured by Manamed, Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ManaMed Inc - Primary ID INVALID PRODUCT
Device Regulatory Overview
The ManaMed Inc (Model/Catalog Number: INVALID PRODUCT) is a medical device manufactured by Manamed, Inc.. This product is indexed under FDA Product Code / Category Classification KYR within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- INVALID PRODUCT
- Product Code / EMDN
- KYR
- Device Name
- This device is universal, this product does not exist. Cannot delete record
- Database Sync Date
- 2026-08-09 09:12:28
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 ManaMed Inc?
The registered manufacturer of record for ManaMed Inc is Manamed, Inc..
What is the Primary UDI-DI identifier for ManaMed Inc?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is INVALID PRODUCT.
What classification code is assigned to this device?
This device is registered under product classification code KYR.
Similar Classification Devices (KYR)
Other Devices by Manamed, Inc.
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