BROCHE (UDI 08698898295909)
Manufactured by Nurteks Tekstil ve Medikal Sanayi Dıs Ticaret Anonim Sirketi
Device Regulatory Overview
The BROCHE (Model/Catalog Number: LG103) is a medical device manufactured by Nurteks Tekstil ve Medikal Sanayi Dıs Ticaret Anonim Sirketi. This product is indexed under FDA Product Code / Category Classification T01010102 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- LG103
- Product Code / EMDN
- T01010102
- Device Name
- NON-STERILE POWDER-FREE LATEX EXAMINATION GLOVES SİZE XS,S,M,L,XL
- Database Sync Date
- 2026-08-09 16:44:47
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 BROCHE?
The registered manufacturer of record for BROCHE is Nurteks Tekstil ve Medikal Sanayi Dıs Ticaret Anonim Sirketi.
What is the Primary UDI-DI identifier for BROCHE?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08698898295909.
What classification code is assigned to this device?
This device is registered under product classification code T01010102.
Similar Classification Devices (T01010102)
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