eudamed_udi
Primary ID: 04038155010915
4er Pelotte (UDI 04038155010915)
Manufactured by TIGGES-Zours GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for 4er Pelotte - Primary ID 04038155010915
Device Regulatory Overview
The 4er Pelotte (Model/Catalog Number: 01091) 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
- 01091
- Product Code / EMDN
- Y060380
- Device Name
- TIGGES/T-FLEX
- 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 4er Pelotte?
The registered manufacturer of record for 4er Pelotte is TIGGES-Zours GmbH.
What is the Primary UDI-DI identifier for 4er Pelotte?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04038155010915.
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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