BA 40303 XS / NEOPRENE HINGED KNEE BRACE OPEN FRONT XS (UDI 08682495018535)
Manufactured by BİOAKTİF TIBBİ ÜRÜNLER VE TEKNİK TEKSTİL SAN. TİC. LTD. ŞTİ.
Device Regulatory Overview
The BA 40303 XS / NEOPRENE HINGED KNEE BRACE OPEN FRONT XS (Model/Catalog Number: BA 40303 XS) 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 Y061209 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- BA 40303 XS
- Product Code / EMDN
- Y061209
- Device Name
- KNEE BRACE SUPPORTS
- Database Sync Date
- 2026-08-09 16:30:07
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 BA 40303 XS / NEOPRENE HINGED KNEE BRACE OPEN FRONT XS?
The registered manufacturer of record for BA 40303 XS / NEOPRENE HINGED KNEE BRACE OPEN FRONT XS is BİOAKTİF TIBBİ ÜRÜNLER VE TEKNİK TEKSTİL SAN. TİC. LTD. ŞTİ..
What is the Primary UDI-DI identifier for BA 40303 XS / NEOPRENE HINGED KNEE BRACE OPEN FRONT XS?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08682495018535.
What classification code is assigned to this device?
This device is registered under product classification code Y061209.
Similar Classification Devices (Y061209)
Other Devices by BİOAKTİF TIBBİ ÜRÜNLER VE TEKNİK TEKSTİL SAN. TİC. LTD. ŞTİ.
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