gudid
Primary ID: 702
Camco (UDI 702)
Manufactured by CAMBRIDGE DIAGNOSTIC PRODUCTS INC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Camco - Primary ID 702
Device Regulatory Overview
The Camco (Model/Catalog Number: 702) is a medical device manufactured by CAMBRIDGE DIAGNOSTIC PRODUCTS INC. This product is indexed under FDA Product Code / Category Classification KQC within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 702
- Product Code / EMDN
- KQC
- Device Name
- Camco Stain Pak - A three step staining system approximating results obtained from either Wright or Wright-Giemsa Stain.
- Database Sync Date
- 2026-08-09 09:04:20
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 Camco?
The registered manufacturer of record for Camco is CAMBRIDGE DIAGNOSTIC PRODUCTS INC.
What is the Primary UDI-DI identifier for Camco?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 702.
What classification code is assigned to this device?
This device is registered under product classification code KQC.
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