TEKNO-CER (UDI 08699328728417)
Manufactured by TEKNO-CER CERRAHİ ALETLER İMALAT SANAYİ VE TİCARET LİMİTED ŞİRKETİ
Device Regulatory Overview
The TEKNO-CER (Model/Catalog Number: T90-978) is a medical device manufactured by TEKNO-CER CERRAHİ ALETLER İMALAT SANAYİ VE TİCARET LİMİTED ŞİRKETİ. This product is indexed under FDA Product Code / Category Classification L08060199 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- T90-978
- Product Code / EMDN
- L08060199
- Device Name
- DILATOR
- Database Sync Date
- 2026-08-09 16:28:46
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 TEKNO-CER?
The registered manufacturer of record for TEKNO-CER is TEKNO-CER CERRAHİ ALETLER İMALAT SANAYİ VE TİCARET LİMİTED ŞİRKETİ.
What is the Primary UDI-DI identifier for TEKNO-CER?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08699328728417.
What classification code is assigned to this device?
This device is registered under product classification code L08060199.
Similar Classification Devices (L08060199)
Other Devices by TEKNO-CER CERRAHİ ALETLER İMALAT SANAYİ VE TİCARET LİMİTED ŞİRKETİ
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