eudamed_udi
Primary ID: 03701140205528
PANST ASS NTISS 2T URGO ROSSIGNOL (18)-1 (UDI 03701140205528)
Manufactured by SECURIMED
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for PANST ASS NTISS 2T URGO ROSSIGNOL (18)-1 - Primary ID 03701140205528
Device Regulatory Overview
The PANST ASS NTISS 2T URGO ROSSIGNOL (18)-1 (Model/Catalog Number: 3500) is a medical device manufactured by SECURIMED. This product is indexed under FDA Product Code / Category Classification M050199 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 3500
- Product Code / EMDN
- M050199
- Device Name
- PANSEMENTS
- Database Sync Date
- 2026-08-09 16:49:06
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 PANST ASS NTISS 2T URGO ROSSIGNOL (18)-1?
The registered manufacturer of record for PANST ASS NTISS 2T URGO ROSSIGNOL (18)-1 is SECURIMED.
What is the Primary UDI-DI identifier for PANST ASS NTISS 2T URGO ROSSIGNOL (18)-1?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03701140205528.
What classification code is assigned to this device?
This device is registered under product classification code M050199.
Similar Classification Devices (M050199)
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