gudid
Primary ID: PRO-24
PlayMakar (UDI PRO-24)
Manufactured by PLAYMAKAR INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for PlayMakar - Primary ID PRO-24
Device Regulatory Overview
The PlayMakar (Model/Catalog Number: PRO-24) is a medical device manufactured by PLAYMAKAR INC.. This product is indexed under FDA Product Code / Category Classification GXY within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- PRO-24
- Product Code / EMDN
- GXY
- Device Name
- PLAYMAKAR SPORT SNAP ELECTRODES, 2" x 4", 2/Pack
- Database Sync Date
- 2026-08-09 09:49:28
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 PlayMakar?
The registered manufacturer of record for PlayMakar is PLAYMAKAR INC..
What is the Primary UDI-DI identifier for PlayMakar?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is PRO-24.
What classification code is assigned to this device?
This device is registered under product classification code GXY.
Similar Classification Devices (GXY)
Other Devices by PLAYMAKAR INC.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint