eudamed_udi
Primary ID: 06975085648499
CITOTEST (UDI 06975085648499)
Manufactured by CITOTEST LABWARE MANUFACTURING CO.,LTD
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for CITOTEST - Primary ID 06975085648499
Device Regulatory Overview
The CITOTEST (Model/Catalog Number: 2120-1406) is a medical device manufactured by CITOTEST LABWARE MANUFACTURING CO.,LTD. This product is indexed under FDA Product Code / Category Classification A1101 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 2120-1406
- Product Code / EMDN
- A1101
- Device Name
- Classical swabs
- Database Sync Date
- 2026-08-09 16:29:23
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 CITOTEST?
The registered manufacturer of record for CITOTEST is CITOTEST LABWARE MANUFACTURING CO.,LTD.
What is the Primary UDI-DI identifier for CITOTEST?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06975085648499.
What classification code is assigned to this device?
This device is registered under product classification code A1101.
Similar Classification Devices (A1101)
Other Devices by CITOTEST LABWARE MANUFACTURING CO.,LTD
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint