gudid
Primary ID: 07103300/S
07103300/S (UDI 07103300/S)
Manufactured by ELCAM MEDICAL ITALY SPA
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for 07103300/S - Primary ID 07103300/S
Device Regulatory Overview
The 07103300/S (Model/Catalog Number: 07103300/S) is a medical device manufactured by ELCAM MEDICAL ITALY SPA. This product is indexed under FDA Product Code / Category Classification FJK within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 07103300/S
- Product Code / EMDN
- FJK
- Device Name
- Recirculating FLL connector with protective vented cap and closed cap
- Database Sync Date
- 2026-08-09 09:04:32
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 07103300/S?
The registered manufacturer of record for 07103300/S is ELCAM MEDICAL ITALY SPA.
What is the Primary UDI-DI identifier for 07103300/S?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 07103300/S.
What classification code is assigned to this device?
This device is registered under product classification code FJK.
Similar Classification Devices (FJK)
Other Devices by ELCAM MEDICAL ITALY SPA
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