ARNES ABDOMINAL Y PIEZA PERINEAL ARNETEC T.1 M: 94-182 ; ABDOMINAL BELT AND PERINEUM PIECE (UDI 08435025985919)
Manufactured by Orliman, S.L.U.
Device Regulatory Overview
The ARNES ABDOMINAL Y PIEZA PERINEAL ARNETEC T.1 M: 94-182 ; ABDOMINAL BELT AND PERINEUM PIECE (Model/Catalog Number: 1005R#1) is a medical device manufactured by Orliman, S.L.U.. This product is indexed under FDA Product Code / Category Classification Y180999 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 1005R#1
- Product Code / EMDN
- Y180999
- Device Name
- Arneses
- Database Sync Date
- 2026-08-09 16:48:26
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 ARNES ABDOMINAL Y PIEZA PERINEAL ARNETEC T.1 M: 94-182 ; ABDOMINAL BELT AND PERINEUM PIECE?
The registered manufacturer of record for ARNES ABDOMINAL Y PIEZA PERINEAL ARNETEC T.1 M: 94-182 ; ABDOMINAL BELT AND PERINEUM PIECE is Orliman, S.L.U..
What is the Primary UDI-DI identifier for ARNES ABDOMINAL Y PIEZA PERINEAL ARNETEC T.1 M: 94-182 ; ABDOMINAL BELT AND PERINEUM PIECE?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08435025985919.
What classification code is assigned to this device?
This device is registered under product classification code Y180999.
Similar Classification Devices (Y180999)
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