eudamed_udi
Primary ID: D-8901117HPK0123KYQM
Huf Puf Kit (UDI D-8901117HPK0123KYQM)
Manufactured by Cipla Limited
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Huf Puf Kit - Primary ID D-8901117HPK0123KYQM
Device Regulatory Overview
The Huf Puf Kit (Model/Catalog Number: Not Applicable for Huf Puf Kit) is a medical device manufactured by Cipla Limited. This product is indexed under FDA Product Code / Category Classification R03010399 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- Not Applicable for Huf Puf Kit
- Product Code / EMDN
- R03010399
- Device Name
- Huf Puf Kit (spacer + mask)
- Database Sync Date
- 2026-08-09 17:20:02
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 Huf Puf Kit?
The registered manufacturer of record for Huf Puf Kit is Cipla Limited.
What is the Primary UDI-DI identifier for Huf Puf Kit?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is D-8901117HPK0123KYQM.
What classification code is assigned to this device?
This device is registered under product classification code R03010399.
Similar Classification Devices (R03010399)
Other Devices by Cipla Limited
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