gudid
Primary ID: 16100
Precept (UDI 16100)
Manufactured by PRECEPT MEDICAL PRODUCTS, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Precept - Primary ID 16100
Device Regulatory Overview
The Precept (Model/Catalog Number: 16100) is a medical device manufactured by PRECEPT MEDICAL PRODUCTS, INC.. This product is indexed under FDA Product Code / Category Classification KYR within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 16100
- Product Code / EMDN
- KYR
- Device Name
- Premium Cold Pack
- Database Sync Date
- 2026-08-09 09:46:39
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 Precept?
The registered manufacturer of record for Precept is PRECEPT MEDICAL PRODUCTS, INC..
What is the Primary UDI-DI identifier for Precept?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 16100.
What classification code is assigned to this device?
This device is registered under product classification code KYR.
Similar Classification Devices (KYR)
Other Devices by PRECEPT MEDICAL PRODUCTS, INC.
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