Y 1208-STN / VISCO REFLUX PILLOW SIZE STANDARD (UDI 08682132217581)
Manufactured by EFAMED ORTOPEDİ MEDİKAL ÜRÜNLER TİC SAN LTD ŞTİ
Device Regulatory Overview
The Y 1208-STN / VISCO REFLUX PILLOW SIZE STANDARD (Model/Catalog Number: Y 1208-STN) is a medical device manufactured by EFAMED ORTOPEDİ MEDİKAL ÜRÜNLER TİC SAN LTD ŞTİ. This product is indexed under FDA Product Code / Category Classification Y180999 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- Y 1208-STN
- Product Code / EMDN
- Y180999
- Device Name
- PILLOWS , SEAT CUSHIONS LUMBER CUSHIONS
- Database Sync Date
- 2026-08-09 16:30:29
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 Y 1208-STN / VISCO REFLUX PILLOW SIZE STANDARD?
The registered manufacturer of record for Y 1208-STN / VISCO REFLUX PILLOW SIZE STANDARD is EFAMED ORTOPEDİ MEDİKAL ÜRÜNLER TİC SAN LTD ŞTİ.
What is the Primary UDI-DI identifier for Y 1208-STN / VISCO REFLUX PILLOW SIZE STANDARD?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08682132217581.
What classification code is assigned to this device?
This device is registered under product classification code Y180999.
Similar Classification Devices (Y180999)
Other Devices by EFAMED ORTOPEDİ MEDİKAL ÜRÜNLER TİC SAN LTD ŞTİ
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