eudamed_udi
Primary ID: 04270002229822
„Pia“ von BECKER® (UDI 04270002229822)
Manufactured by Becker GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for „Pia“ von BECKER® - Primary ID 04270002229822
Device Regulatory Overview
The „Pia“ von BECKER® (Model/Catalog Number: 42 700022298LiegenFM) is a medical device manufactured by Becker GmbH. This product is indexed under FDA Product Code / Category Classification Y1803 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 42 700022298LiegenFM
- Product Code / EMDN
- Y1803
- Device Name
- „Lisa“ von BECKER® und „Pia“ von BECKER®
- Database Sync Date
- 2026-08-09 18:03:34
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 „Pia“ von BECKER®?
The registered manufacturer of record for „Pia“ von BECKER® is Becker GmbH.
What is the Primary UDI-DI identifier for „Pia“ von BECKER®?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04270002229822.
What classification code is assigned to this device?
This device is registered under product classification code Y1803.
Similar Classification Devices (Y1803)
Other Devices by Becker GmbH
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