eudamed_udi
Primary ID: 08681376083617
ASELTECH (UDI 08681376083617)
Manufactured by Asel Tibbi Aletler A.S.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ASELTECH - Primary ID 08681376083617
Device Regulatory Overview
The ASELTECH (Model/Catalog Number: BV-3865) is a medical device manufactured by Asel Tibbi Aletler A.S.. This product is indexed under FDA Product Code / Category Classification L0922 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- BV-3865
- Product Code / EMDN
- L0922
- Device Name
- SEPARATOR
- Database Sync Date
- 2026-08-09 16:28:48
Full Regulatory Attributes
π Token Gated
{
"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 ASELTECH?
The registered manufacturer of record for ASELTECH is Asel Tibbi Aletler A.S..
What is the Primary UDI-DI identifier for ASELTECH?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08681376083617.
What classification code is assigned to this device?
This device is registered under product classification code L0922.
Similar Classification Devices (L0922)
Other Devices by Asel Tibbi Aletler A.S.
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