eudamed_udi
Primary ID: 08800065172009
CERA-CHEK™ 1070 Glucose Control Solution (UDI 08800065172009)
Manufactured by GC MEDIS Corp.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for CERA-CHEK™ 1070 Glucose Control Solution - Primary ID 08800065172009
Device Regulatory Overview
The CERA-CHEK™ 1070 Glucose Control Solution (Model/Catalog Number: G300C10) is a medical device manufactured by GC MEDIS Corp.. This product is indexed under FDA Product Code / Category Classification W0101050205 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- G300C10
- Product Code / EMDN
- W0101050205
- Device Name
- CERA-CHEK™ 1070 Glucose Control Solution
- Database Sync Date
- 2026-08-09 17:38:49
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 CERA-CHEK™ 1070 Glucose Control Solution?
The registered manufacturer of record for CERA-CHEK™ 1070 Glucose Control Solution is GC MEDIS Corp..
What is the Primary UDI-DI identifier for CERA-CHEK™ 1070 Glucose Control Solution?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08800065172009.
What classification code is assigned to this device?
This device is registered under product classification code W0101050205.
Similar Classification Devices (W0101050205)
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