gudid
Primary ID: R124102
ACT II Dual Transport PK/10 (UDI R124102)
Manufactured by REMEL, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ACT II Dual Transport PK/10 - Primary ID R124102
Device Regulatory Overview
The ACT II Dual Transport PK/10 (Model/Catalog Number: R124102) is a medical device manufactured by REMEL, INC.. This product is indexed under FDA Product Code / Category Classification JSL within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- R124102
- Product Code / EMDN
- JSL
- Device Name
- ACT II
- Database Sync Date
- 2026-08-09 09:13:54
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 ACT II Dual Transport PK/10?
The registered manufacturer of record for ACT II Dual Transport PK/10 is REMEL, INC..
What is the Primary UDI-DI identifier for ACT II Dual Transport PK/10?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is R124102.
What classification code is assigned to this device?
This device is registered under product classification code JSL.
Similar Classification Devices (JSL)
Other Devices by REMEL, INC.
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