eudamed_udi
Primary ID: D-KR2DD
Crypto/Giardia CEL IFA (UDI D-KR2DD)
Manufactured by Cellabs Pty Ltd
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Crypto/Giardia CEL IFA - Primary ID D-KR2DD
Device Regulatory Overview
The Crypto/Giardia CEL IFA (Model/Catalog Number: KR2) is a medical device manufactured by Cellabs Pty Ltd. This product is indexed under FDA Product Code / Category Classification W0105090499 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- KR2
- Product Code / EMDN
- W0105090499
- Device Name
- Crypto/Giardia CEL IFA
- Database Sync Date
- 2026-08-09 16:29:40
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 Crypto/Giardia CEL IFA?
The registered manufacturer of record for Crypto/Giardia CEL IFA is Cellabs Pty Ltd.
What is the Primary UDI-DI identifier for Crypto/Giardia CEL IFA?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is D-KR2DD.
What classification code is assigned to this device?
This device is registered under product classification code W0105090499.
Similar Classification Devices (W0105090499)
Other Devices by Cellabs Pty Ltd
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