Reinforced Floor Drape 78*300 (UDI 08685260300026)
Manufactured by MHK MEDİKAL TEKSTİL SAN VE TİC.LTD.ŞTİ
Device Regulatory Overview
The Reinforced Floor Drape 78*300 (Model/Catalog Number: MHK-2990046) is a medical device manufactured by MHK MEDİKAL TEKSTİL SAN VE TİC.LTD.ŞTİ. This product is indexed under FDA Product Code / Category Classification T0210 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- MHK-2990046
- Product Code / EMDN
- T0210
- Device Name
- PATIENT GOWN (SHORT SLEEVED) S
- Database Sync Date
- 2026-08-09 16:30:30
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 Reinforced Floor Drape 78*300?
The registered manufacturer of record for Reinforced Floor Drape 78*300 is MHK MEDİKAL TEKSTİL SAN VE TİC.LTD.ŞTİ.
What is the Primary UDI-DI identifier for Reinforced Floor Drape 78*300?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08685260300026.
What classification code is assigned to this device?
This device is registered under product classification code T0210.
Similar Classification Devices (T0210)
Other Devices by MHK MEDİKAL TEKSTİL SAN VE TİC.LTD.ŞTİ
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