ROCCER BATTOM SOLE SLIPPER WOMEN BLACK / 39 (UDI 08680702036167)
Manufactured by BEYAZGRUP SAĞLIK ÜRÜNLERİ İMALAT SANAYİ VE TİCARET LİMİTED ŞİRKETİ
Device Regulatory Overview
The ROCCER BATTOM SOLE SLIPPER WOMEN BLACK / 39 (Model/Catalog Number: ML-1020-39) is a medical device manufactured by BEYAZGRUP SAĞLIK ÜRÜNLERİ İMALAT SANAYİ VE TİCARET LİMİTED ŞİRKETİ. This product is indexed under FDA Product Code / Category Classification V080399 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- ML-1020-39
- Product Code / EMDN
- V080399
- Device Name
- MEDICAL SLIPPERS
- Database Sync Date
- 2026-08-09 16:28:52
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 ROCCER BATTOM SOLE SLIPPER WOMEN BLACK / 39?
The registered manufacturer of record for ROCCER BATTOM SOLE SLIPPER WOMEN BLACK / 39 is BEYAZGRUP SAĞLIK ÜRÜNLERİ İMALAT SANAYİ VE TİCARET LİMİTED ŞİRKETİ.
What is the Primary UDI-DI identifier for ROCCER BATTOM SOLE SLIPPER WOMEN BLACK / 39?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08680702036167.
What classification code is assigned to this device?
This device is registered under product classification code V080399.
Similar Classification Devices (V080399)
Other Devices by BEYAZGRUP SAĞLIK ÜRÜNLERİ İMALAT SANAYİ VE TİCARET LİMİTED ŞİRKETİ
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