BA 300 XXL / ABDOMINAFIX Postoperative Elastic Corset (UDI 08682495002947)
Manufactured by BİOAKTİF TIBBİ ÜRÜNLER VE TEKNİK TEKSTİL SAN. TİC. LTD. ŞTİ.
Device Regulatory Overview
The BA 300 XXL / ABDOMINAFIX Postoperative Elastic Corset (Model/Catalog Number: BA 300 XXL) is a medical device manufactured by BİOAKTİF TIBBİ ÜRÜNLER VE TEKNİK TEKSTİL SAN. TİC. LTD. ŞTİ.. This product is indexed under FDA Product Code / Category Classification Y060403 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- BA 300 XXL
- Product Code / EMDN
- Y060403
- Device Name
- CORSET SUPPORTS
- Database Sync Date
- 2026-08-09 16:30:14
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 BA 300 XXL / ABDOMINAFIX Postoperative Elastic Corset?
The registered manufacturer of record for BA 300 XXL / ABDOMINAFIX Postoperative Elastic Corset is BİOAKTİF TIBBİ ÜRÜNLER VE TEKNİK TEKSTİL SAN. TİC. LTD. ŞTİ..
What is the Primary UDI-DI identifier for BA 300 XXL / ABDOMINAFIX Postoperative Elastic Corset?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08682495002947.
What classification code is assigned to this device?
This device is registered under product classification code Y060403.
Similar Classification Devices (Y060403)
Other Devices by BİOAKTİF TIBBİ ÜRÜNLER VE TEKNİK TEKSTİL SAN. TİC. LTD. ŞTİ.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint