gudid
Primary ID: ACSK38879
Therapak (UDI ACSK38879)
Manufactured by Therapak LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Therapak - Primary ID ACSK38879
Device Regulatory Overview
The Therapak (Model/Catalog Number: ACSK38879) is a medical device manufactured by Therapak LLC. This product is indexed under FDA Product Code / Category Classification NNK within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- ACSK38879
- Product Code / EMDN
- NNK
- Device Name
- StoneScreen Collection and Transport Kit (CS/16)
- Database Sync Date
- 2026-08-09 09:10:29
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 Therapak?
The registered manufacturer of record for Therapak is Therapak LLC.
What is the Primary UDI-DI identifier for Therapak?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is ACSK38879.
What classification code is assigned to this device?
This device is registered under product classification code NNK.
Similar Classification Devices (NNK)
Other Devices by Therapak LLC
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint