gudid
Primary ID: PRO-1000
PlayMakar (UDI PRO-1000)
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-1000
Device Regulatory Overview
The PlayMakar (Model/Catalog Number: PRO-1000) is a medical device manufactured by PLAYMAKAR INC.. This product is indexed under FDA Product Code / Category Classification NYN within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- PRO-1000
- Product Code / EMDN
- NYN
- Device Name
- PLAYMAKAR PRO STRENGTH AND RECOVERY SYSTEM
- Database Sync Date
- 2026-08-09 09:49:28
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 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-1000.
What classification code is assigned to this device?
This device is registered under product classification code NYN.
Similar Classification Devices (NYN)
Other Devices by PLAYMAKAR INC.
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