gudid
Primary ID: 1746-01
Innomed, Inc. (UDI 1746-01)
Manufactured by INNOMED, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Innomed, Inc. - Primary ID 1746-01
Device Regulatory Overview
The Innomed, Inc. (Model/Catalog Number: 1746-01) is a medical device manufactured by INNOMED, INC.. This product is indexed under FDA Product Code / Category Classification KIL within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 1746-01
- Product Code / EMDN
- KIL
- Device Name
- Silicone Hand
- Database Sync Date
- 2026-08-09 09:12:06
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 Innomed, Inc.?
The registered manufacturer of record for Innomed, Inc. is INNOMED, INC..
What is the Primary UDI-DI identifier for Innomed, Inc.?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 1746-01.
What classification code is assigned to this device?
This device is registered under product classification code KIL.
Similar Classification Devices (KIL)
Other Devices by INNOMED, INC.
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