TEKNOMEK (UDI 08680548901223)
Manufactured by TEKNOMEK MEDİKAL MALZEMELERİ SAN. ve TİC. LTD. ŞTİ.
Device Regulatory Overview
The TEKNOMEK (Model/Catalog Number: CH126) is a medical device manufactured by TEKNOMEK MEDİKAL MALZEMELERİ SAN. ve TİC. LTD. ŞTİ.. This product is indexed under FDA Product Code / Category Classification A01010199 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- CH126
- Product Code / EMDN
- A01010199
- Device Name
- Cortical Cleaving Hydrodissector (Grabow) (0.40 x 22mm, 27G)
- Database Sync Date
- 2026-08-09 16:29:44
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of TEKNOMEK?
The registered manufacturer of record for TEKNOMEK is TEKNOMEK MEDİKAL MALZEMELERİ SAN. ve TİC. LTD. ŞTİ..
What is the Primary UDI-DI identifier for TEKNOMEK?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08680548901223.
What classification code is assigned to this device?
This device is registered under product classification code A01010199.
Similar Classification Devices (A01010199)
Other Devices by TEKNOMEK MEDİKAL MALZEMELERİ SAN. ve TİC. LTD. ŞTİ.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint