gudid
Primary ID: 5372
Helena Ristocetin - 10 mg/mL (UDI 5372)
Manufactured by HELENA LABORATORIES CORPORATION
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Helena Ristocetin - 10 mg/mL - Primary ID 5372
Device Regulatory Overview
The Helena Ristocetin - 10 mg/mL (Model/Catalog Number: 5372) is a medical device manufactured by HELENA LABORATORIES CORPORATION. This product is indexed under FDA Product Code / Category Classification GGP within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 5372
- Product Code / EMDN
- GGP
- Device Name
- Database Sync Date
- 2026-08-09 09:36:16
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 Helena Ristocetin - 10 mg/mL?
The registered manufacturer of record for Helena Ristocetin - 10 mg/mL is HELENA LABORATORIES CORPORATION.
What is the Primary UDI-DI identifier for Helena Ristocetin - 10 mg/mL?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 5372.
What classification code is assigned to this device?
This device is registered under product classification code GGP.
Similar Classification Devices (GGP)
Other Devices by HELENA LABORATORIES CORPORATION
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