AYSET (UDI 08697427709092)
Manufactured by AYSET TIBBI URUNLER VE PLASTIK TEKSTIL ELEKTRONIK GIDA TEMIZLIK MADDELERI INSAAT MUTEAHHITLIK SANAYI A.S.
Device Regulatory Overview
The AYSET (Model/Catalog Number: 70651) is a medical device manufactured by AYSET TIBBI URUNLER VE PLASTIK TEKSTIL ELEKTRONIK GIDA TEMIZLIK MADDELERI INSAAT MUTEAHHITLIK SANAYI A.S.. This product is indexed under FDA Product Code / Category Classification W050101010202 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 70651
- Product Code / EMDN
- W050101010202
- Device Name
- 4 ml Z No Additive Blood Collection Tube
- Database Sync Date
- 2026-08-09 16:48:21
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 AYSET?
The registered manufacturer of record for AYSET is AYSET TIBBI URUNLER VE PLASTIK TEKSTIL ELEKTRONIK GIDA TEMIZLIK MADDELERI INSAAT MUTEAHHITLIK SANAYI A.S..
What is the Primary UDI-DI identifier for AYSET?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08697427709092.
What classification code is assigned to this device?
This device is registered under product classification code W050101010202.
Similar Classification Devices (W050101010202)
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