gudid
Primary ID: 00101F
VIROTROL (UDI 00101F)
Manufactured by BIO-RAD LABORATORIES, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for VIROTROL - Primary ID 00101F
Device Regulatory Overview
The VIROTROL (Model/Catalog Number: 00101F) is a medical device manufactured by BIO-RAD LABORATORIES, INC.. This product is indexed under FDA Product Code / Category Classification KSF within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 00101F
- Product Code / EMDN
- KSF
- Device Name
- VIROTROL I (An unassayed (human) serological control.)
- Database Sync Date
- 2026-08-09 09:48:17
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 VIROTROL?
The registered manufacturer of record for VIROTROL is BIO-RAD LABORATORIES, INC..
What is the Primary UDI-DI identifier for VIROTROL?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00101F.
What classification code is assigned to this device?
This device is registered under product classification code KSF.
Similar Classification Devices (KSF)
Other Devices by BIO-RAD LABORATORIES, INC.
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