aidplast (UDI 08682132500836)
Manufactured by VİCTOREKS TIBBİ SAĞLIK ÜRÜNLERİ İÇ VE DIŞ TİC. SAN. LTD. ŞTİ.
Device Regulatory Overview
The aidplast (Model/Catalog Number: V3105 V3105) is a medical device manufactured by VİCTOREKS TIBBİ SAĞLIK ÜRÜNLERİ İÇ VE DIŞ TİC. SAN. LTD. ŞTİ.. This product is indexed under FDA Product Code / Category Classification M050199,M0599 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- V3105 V3105
- Product Code / EMDN
- M050199,M0599
- Device Name
- Surgical Tape(plaster)
- Database Sync Date
- 2026-08-09 16:28:50
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 aidplast?
The registered manufacturer of record for aidplast is VİCTOREKS TIBBİ SAĞLIK ÜRÜNLERİ İÇ VE DIŞ TİC. SAN. LTD. ŞTİ..
What is the Primary UDI-DI identifier for aidplast?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08682132500836.
What classification code is assigned to this device?
This device is registered under product classification code M050199,M0599.
Similar Classification Devices (M050199,M0599)
Other Devices by VİCTOREKS TIBBİ SAĞLIK ÜRÜNLERİ İÇ VE DIŞ TİC. SAN. LTD. ŞTİ.
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