eudamed_udi
Primary ID: 07330530004852
SKRUVNIPPEL SPETS 6X17 (UDI 07330530004852)
Manufactured by Haco Tellus AB
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for SKRUVNIPPEL SPETS 6X17 - Primary ID 07330530004852
Device Regulatory Overview
The SKRUVNIPPEL SPETS 6X17 (Model/Catalog Number: 4100029) is a medical device manufactured by Haco Tellus AB. This product is indexed under FDA Product Code / Category Classification Y122403 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 4100029
- Product Code / EMDN
- Y122403
- Device Name
- BROMSWIRE 900/1170 KARL OSKAR
- Database Sync Date
- 2026-08-09 16:29:03
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 SKRUVNIPPEL SPETS 6X17?
The registered manufacturer of record for SKRUVNIPPEL SPETS 6X17 is Haco Tellus AB.
What is the Primary UDI-DI identifier for SKRUVNIPPEL SPETS 6X17?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 07330530004852.
What classification code is assigned to this device?
This device is registered under product classification code Y122403.
Similar Classification Devices (Y122403)
Other Devices by Haco Tellus AB
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