Rheumatoid factor (RF), 5 mL Latex, 1 mL Positive control, 1 mL Negative Control (UDI D-084360385655653HB)
Manufactured by Chronolab Systems, S.L.
Device Regulatory Overview
The Rheumatoid factor (RF), 5 mL Latex, 1 mL Positive control, 1 mL Negative Control (Model/Catalog Number: 101-0218) is a medical device manufactured by Chronolab Systems, S.L.. This product is indexed under FDA Product Code / Category Classification W01021110 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 101-0218
- Product Code / EMDN
- W01021110
- Device Name
- Rheumatoid factor (RF), 5 mL Latex, 1 mL Positive control, 1 mL Negative Control
- Database Sync Date
- 2026-08-09 16:29:33
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 Rheumatoid factor (RF), 5 mL Latex, 1 mL Positive control, 1 mL Negative Control?
The registered manufacturer of record for Rheumatoid factor (RF), 5 mL Latex, 1 mL Positive control, 1 mL Negative Control is Chronolab Systems, S.L..
What is the Primary UDI-DI identifier for Rheumatoid factor (RF), 5 mL Latex, 1 mL Positive control, 1 mL Negative Control?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is D-084360385655653HB.
What classification code is assigned to this device?
This device is registered under product classification code W01021110.
Similar Classification Devices (W01021110)
Other Devices by Chronolab Systems, S.L.
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