gudid
Primary ID: 10mL
Lyophilized Platelets (UDI 10mL)
Manufactured by Bio/Data Corporation
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Lyophilized Platelets - Primary ID 10mL
Device Regulatory Overview
The Lyophilized Platelets (Model/Catalog Number: 10mL) is a medical device manufactured by Bio/Data Corporation. This product is indexed under FDA Product Code / Category Classification GGP within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 10mL
- Product Code / EMDN
- GGP
- Device Name
- Database Sync Date
- 2026-08-09 09:04:02
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Lyophilized Platelets?
The registered manufacturer of record for Lyophilized Platelets is Bio/Data Corporation.
What is the Primary UDI-DI identifier for Lyophilized Platelets?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 10mL.
What classification code is assigned to this device?
This device is registered under product classification code GGP.
Similar Classification Devices (GGP)
Other Devices by Bio/Data Corporation
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint