eudamed_udi
Primary ID: 04048486245962
Lendenpelotte 23 cm (UDI 04048486245962)
Manufactured by Werkmeister GmbH + Co. KG
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Lendenpelotte 23 cm - Primary ID 04048486245962
Device Regulatory Overview
The Lendenpelotte 23 cm (Model/Catalog Number: 40523) is a medical device manufactured by Werkmeister GmbH + Co. KG. This product is indexed under FDA Product Code / Category Classification Y060380 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 40523
- Product Code / EMDN
- Y060380
- Device Name
- Rumpfstützorthese
- Database Sync Date
- 2026-08-09 16:46:57
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 Lendenpelotte 23 cm?
The registered manufacturer of record for Lendenpelotte 23 cm is Werkmeister GmbH + Co. KG.
What is the Primary UDI-DI identifier for Lendenpelotte 23 cm?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04048486245962.
What classification code is assigned to this device?
This device is registered under product classification code Y060380.
Similar Classification Devices (Y060380)
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