eudamed_udi
Primary ID: D-060062877E
Sinulan Forte Express Junior (UDI D-060062877E)
Manufactured by S.I.I.T. srl
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Sinulan Forte Express Junior - Primary ID D-060062877E
Device Regulatory Overview
The Sinulan Forte Express Junior (Model/Catalog Number: OC01A - Mild hypertonic solution) is a medical device manufactured by S.I.I.T. srl. This product is indexed under FDA Product Code / Category Classification Q030199 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- OC01A - Mild hypertonic solution
- Product Code / EMDN
- Q030199
- Device Name
- Sinulan Forte Express Junior
- Database Sync Date
- 2026-08-09 16:30:01
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 Sinulan Forte Express Junior?
The registered manufacturer of record for Sinulan Forte Express Junior is S.I.I.T. srl.
What is the Primary UDI-DI identifier for Sinulan Forte Express Junior?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is D-060062877E.
What classification code is assigned to this device?
This device is registered under product classification code Q030199.
Similar Classification Devices (Q030199)
Other Devices by S.I.I.T. srl
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint