eudamed_udi
Primary ID: 00848838022333
HIPPURATE DISK (UDI 00848838022333)
Manufactured by Remel, Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for HIPPURATE DISK - Primary ID 00848838022333
Device Regulatory Overview
The HIPPURATE DISK (Model/Catalog Number: R21085) is a medical device manufactured by Remel, Inc.. This product is indexed under FDA Product Code / Category Classification W0104080208 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- R21085
- Product Code / EMDN
- W0104080208
- Device Name
- HIPPURATE DISK
- Database Sync Date
- 2026-08-09 16:46:03
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 HIPPURATE DISK?
The registered manufacturer of record for HIPPURATE DISK is Remel, Inc..
What is the Primary UDI-DI identifier for HIPPURATE DISK?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00848838022333.
What classification code is assigned to this device?
This device is registered under product classification code W0104080208.
Similar Classification Devices (W0104080208)
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