gudid
Primary ID: 0010080
PUMA-G System (UDI 0010080)
Manufactured by Coaptech, Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for PUMA-G System - Primary ID 0010080
Device Regulatory Overview
The PUMA-G System (Model/Catalog Number: 0010080) is a medical device manufactured by Coaptech, Inc.. This product is indexed under FDA Product Code / Category Classification KGC within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 0010080
- Product Code / EMDN
- KGC
- Device Name
- External Magnet in Case
- Database Sync Date
- 2026-08-09 09:58:58
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 PUMA-G System?
The registered manufacturer of record for PUMA-G System is Coaptech, Inc..
What is the Primary UDI-DI identifier for PUMA-G System?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 0010080.
What classification code is assigned to this device?
This device is registered under product classification code KGC.
Similar Classification Devices (KGC)
Other Devices by Coaptech, Inc.
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