eudamed_udi
Primary ID: 06937909307210
OCI (UDI 06937909307210)
Manufactured by CHENGDU OCI MEDICAL DEVICES CO., LTD.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for OCI - Primary ID 06937909307210
Device Regulatory Overview
The OCI (Model/Catalog Number: OCI-HD210L) is a medical device manufactured by CHENGDU OCI MEDICAL DEVICES CO., LTD.. This product is indexed under FDA Product Code / Category Classification F01060103 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- OCI-HD210L
- Product Code / EMDN
- F01060103
- Device Name
- Polyethersulfone Hollow Fiber Hemodialyzer
- Database Sync Date
- 2026-08-09 16:48:33
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 OCI?
The registered manufacturer of record for OCI is CHENGDU OCI MEDICAL DEVICES CO., LTD..
What is the Primary UDI-DI identifier for OCI?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06937909307210.
What classification code is assigned to this device?
This device is registered under product classification code F01060103.
Similar Classification Devices (F01060103)
Other Devices by CHENGDU OCI MEDICAL DEVICES CO., LTD.
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