eudamed_udi
Primary ID: 07330530000847
HPU 16X1.75 / 16X2 SVART RUND (UDI 07330530000847)
Manufactured by Haco Tellus AB
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for HPU 16X1.75 / 16X2 SVART RUND - Primary ID 07330530000847
Device Regulatory Overview
The HPU 16X1.75 / 16X2 SVART RUND (Model/Catalog Number: 3600050) is a medical device manufactured by Haco Tellus AB. This product is indexed under FDA Product Code / Category Classification Y122499 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 3600050
- Product Code / EMDN
- Y122499
- Device Name
- HJUL PE 200X50 ALUFÄLG GRÅ C-179
- Database Sync Date
- 2026-08-09 16:29:18
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 HPU 16X1.75 / 16X2 SVART RUND?
The registered manufacturer of record for HPU 16X1.75 / 16X2 SVART RUND is Haco Tellus AB.
What is the Primary UDI-DI identifier for HPU 16X1.75 / 16X2 SVART RUND?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 07330530000847.
What classification code is assigned to this device?
This device is registered under product classification code Y122499.
Similar Classification Devices (Y122499)
Other Devices by Haco Tellus AB
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