gudid
Primary ID: HWELD-B.DB.00G
WELD B (UDI HWELD-B.DB.00G)
Manufactured by DELCON SRL
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for WELD B - Primary ID HWELD-B.DB.00G
Device Regulatory Overview
The WELD B (Model/Catalog Number: HWELD-B.DB.00G) is a medical device manufactured by DELCON SRL. This product is indexed under FDA Product Code / Category Classification KSD within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- HWELD-B.DB.00G
- Product Code / EMDN
- KSD
- Device Name
- Mobile tube sealer for medical PVC tubes
- Database Sync Date
- 2026-08-09 09:04:33
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 WELD B?
The registered manufacturer of record for WELD B is DELCON SRL.
What is the Primary UDI-DI identifier for WELD B?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is HWELD-B.DB.00G.
What classification code is assigned to this device?
This device is registered under product classification code KSD.
Similar Classification Devices (KSD)
Other Devices by DELCON SRL
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