VACUSERA (UDI M7122346011)
Manufactured by DİSERA TIBBİ MALZEME LOJİSTİK SAN. VE TİC. A.Ş.
Device Regulatory Overview
The VACUSERA (Model/Catalog Number: 234601) is a medical device manufactured by DİSERA TIBBİ MALZEME LOJİSTİK SAN. VE TİC. A.Ş.. This product is indexed under FDA Product Code / Category Classification W050101010201 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 234601
- Product Code / EMDN
- W050101010201
- Device Name
- VACUSERA® 1 ml K2E/K2EDTA Blood Collection Tube
- Database Sync Date
- 2026-08-09 16:28:44
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 VACUSERA?
The registered manufacturer of record for VACUSERA is DİSERA TIBBİ MALZEME LOJİSTİK SAN. VE TİC. A.Ş..
What is the Primary UDI-DI identifier for VACUSERA?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is M7122346011.
What classification code is assigned to this device?
This device is registered under product classification code W050101010201.
Similar Classification Devices (W050101010201)
Other Devices by DİSERA TIBBİ MALZEME LOJİSTİK SAN. VE TİC. A.Ş.
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