eudamed_udi
Primary ID: 04038155543956
LWS-Miederoberteil zur TLO (UDI 04038155543956)
Manufactured by TIGGES-Zours GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for LWS-Miederoberteil zur TLO - Primary ID 04038155543956
Device Regulatory Overview
The LWS-Miederoberteil zur TLO (Model/Catalog Number: 53549-140haut) is a medical device manufactured by TIGGES-Zours GmbH. This product is indexed under FDA Product Code / Category Classification Y060380 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 53549-140haut
- Product Code / EMDN
- Y060380
- Device Name
- TIGGES/T-FLEX
- Database Sync Date
- 2026-08-09 16:29:59
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 LWS-Miederoberteil zur TLO?
The registered manufacturer of record for LWS-Miederoberteil zur TLO is TIGGES-Zours GmbH.
What is the Primary UDI-DI identifier for LWS-Miederoberteil zur TLO?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04038155543956.
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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