gudid
Primary ID: BTT
BTT (UDI BTT)
Manufactured by STERYLAB SRL
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for BTT - Primary ID BTT
Device Regulatory Overview
The BTT (Model/Catalog Number: BTT) is a medical device manufactured by STERYLAB SRL. This product is indexed under FDA Product Code / Category Classification FCG within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- BTT
- Product Code / EMDN
- FCG
- Device Name
- bone-marrow trasplantation needle 11G 9 cm
- Database Sync Date
- 2026-08-09 09:04:33
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 BTT?
The registered manufacturer of record for BTT is STERYLAB SRL.
What is the Primary UDI-DI identifier for BTT?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is BTT.
What classification code is assigned to this device?
This device is registered under product classification code FCG.
Similar Classification Devices (FCG)
Other Devices by STERYLAB SRL
Programmatic Export
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