eudamed_udi
Primary ID: 05944792000013
Sanrotex Medical (UDI 05944792000013)
Manufactured by Bandtex Grup S.R.L.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Sanrotex Medical - Primary ID 05944792000013
Device Regulatory Overview
The Sanrotex Medical (Model/Catalog Number: BTX4040100) is a medical device manufactured by Bandtex Grup S.R.L.. This product is indexed under FDA Product Code / Category Classification M0201010102 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- BTX4040100
- Product Code / EMDN
- M0201010102
- Device Name
- Gauze Swabs
- Database Sync Date
- 2026-08-09 18:09:17
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 Sanrotex Medical?
The registered manufacturer of record for Sanrotex Medical is Bandtex Grup S.R.L..
What is the Primary UDI-DI identifier for Sanrotex Medical?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05944792000013.
What classification code is assigned to this device?
This device is registered under product classification code M0201010102.
Similar Classification Devices (M0201010102)
Other Devices by Bandtex Grup S.R.L.
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