gudid
Primary ID: G56135
Captura (UDI G56135)
Manufactured by COOK INCORPORATED
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Captura - Primary ID G56135
Device Regulatory Overview
The Captura (Model/Catalog Number: G56135) is a medical device manufactured by COOK INCORPORATED. This product is indexed under FDA Product Code / Category Classification KGE within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- G56135
- Product Code / EMDN
- KGE
- Device Name
- Captura Hot Serrated Forceps w/o Spike
- Database Sync Date
- 2026-08-09 09:33:18
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Captura?
The registered manufacturer of record for Captura is COOK INCORPORATED.
What is the Primary UDI-DI identifier for Captura?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is G56135.
What classification code is assigned to this device?
This device is registered under product classification code KGE.
Similar Classification Devices (KGE)
Other Devices by COOK INCORPORATED
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint